Canonical Allele Identifier: CA375821943

Gene: ZMYND11

Linked Data

• dbSNP Id: rs1057518121
• gnomAD v2: 10-294285-C-A
• gnomAD v4: 10-248345-C-A
• MyVariant Identifiers: chr10:g.294285C>A (hg19) ; chr10:g.248345C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.248345C>A , CM000672.2:g.248345C>A	GRCh38
NC_000010.10:g.294285C>A , CM000672.1:g.294285C>A	GRCh37
NC_000010.9:g.284285C>A	NCBI36
NG_029960.1:g.118881C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381584.6:c.*1179C>A	ENSP00000370996.2:n.*1179C>A
ENST00000704295.1:c.1075C>A	ENSP00000515819.1:p.Pro359Thr
ENST00000704301.1:c.1237C>A	ENSP00000515825.1:p.Pro413Thr
ENST00000704303.1:c.1075C>A	ENSP00000515827.1:p.Pro359Thr
ENST00000704306.1:c.*938C>A	ENSP00000515830.1:n.*938C>A
ENST00000704307.1:c.931C>A	ENSP00000515831.1:p.Pro311Thr
ENST00000704315.1:c.1168C>A	ENSP00000515835.1:p.Pro390Thr
ENST00000704335.1:c.1075C>A	ENSP00000515849.1:p.Pro359Thr
ENST00000704338.1:c.754C>A	ENSP00000515850.1:p.Pro252Thr
ENST00000704339.1:c.*372C>A	ENSP00000515851.1:n.*372C>A
ENST00000704343.1:c.1117C>A	ENSP00000515854.1:p.Pro373Thr
ENST00000381604.9:c.1237C>A MANE Select	ENSP00000371017.6:p.Pro413Thr
ENST00000397955.7:c.1282C>A	ENSP00000381046.3:p.Pro428Thr
ENST00000397962.8:c.1237C>A	ENSP00000381053.3:p.Pro413Thr
ENST00000602682.6:c.982C>A	ENSP00000473321.1:p.Pro328Thr
ENST00000627286.2:c.1234C>A	ENSP00000487386.2:p.Pro412Thr
ENST00000309776.8:c.1072C>A	ENSP00000309992.5:p.Pro358Thr
ENST00000381584.5:c.1186C>A	ENSP00000370996.1:p.Pro396Thr
ENST00000381591.5:c.1237C>A	ENSP00000371003.1:p.Pro413Thr
ENST00000381604.8:c.877C>A	ENSP00000371017.5:p.Pro293Thr
ENST00000381607.8:c.1075C>A	ENSP00000371020.5:p.Pro359Thr
ENST00000397959.7:c.982C>A	ENSP00000381050.3:p.Pro328Thr
ENST00000397962.7:c.1237C>A	ENSP00000381053.3:p.Pro413Thr
ENST00000402736.5:c.1144C>A	ENSP00000386010.1:p.Pro382Thr
ENST00000403354.5:c.997C>A	ENSP00000385484.1:p.Pro333Thr
ENST00000473115.1:n.417C>A
ENST00000509513.6:c.1234C>A	ENSP00000424205.2:p.Pro412Thr
ENST00000558098.4:c.1237C>A	ENSP00000452959.1:p.Pro413Thr
ENST00000602682.5:c.982C>A	ENSP00000473321.1:p.Pro328Thr
ENST00000627286.1:c.1186C>A	ENSP00000487386.1:p.Pro396Thr
NM_001202464.1:c.1075C>A	NP_001189393.1:p.Pro359Thr
NM_001202465.1:c.982C>A	NP_001189394.1:p.Pro328Thr
NM_001202466.1:c.1072C>A	NP_001189395.1:p.Pro358Thr
NM_001202467.1:c.1075C>A	NP_001189396.1:p.Pro359Thr
NM_001202468.1:c.1237C>A	NP_001189397.1:p.Pro413Thr
NM_006624.5:c.1237C>A	NP_006615.2:p.Pro413Thr
NM_212479.3:c.1234C>A	NP_997644.2:p.Pro412Thr
XM_005252359.3:c.1237C>A	XP_005252416.1:p.Pro413Thr
XM_005252360.3:c.1234C>A	XP_005252417.1:p.Pro412Thr
XM_005252361.2:c.1075C>A	XP_005252418.1:p.Pro359Thr
XM_005252362.1:c.1075C>A	XP_005252419.1:p.Pro359Thr
XM_006717376.1:c.1075C>A	XP_006717439.1:p.Pro359Thr
XM_011519301.1:c.1186C>A	XP_011517603.1:p.Pro396Thr
XM_011519302.1:c.1072C>A	XP_011517604.1:p.Pro358Thr
NM_001330057.1:c.1186C>A	NP_001316986.1:p.Pro396Thr
XM_005252359.4:c.1237C>A	XP_005252416.1:p.Pro413Thr
XM_005252361.3:c.1075C>A	XP_005252418.1:p.Pro359Thr
XM_005252362.2:c.1075C>A	XP_005252419.1:p.Pro359Thr
XM_006717376.2:c.1075C>A	XP_006717439.1:p.Pro359Thr
XM_017015587.1:c.1237C>A	XP_016871076.1:p.Pro413Thr
XM_017015588.1:c.1237C>A	XP_016871077.1:p.Pro413Thr
XM_017015589.1:c.1237C>A	XP_016871078.1:p.Pro413Thr
XM_017015590.1:c.1237C>A	XP_016871079.1:p.Pro413Thr
XM_017015592.1:c.1075C>A	XP_016871081.1:p.Pro359Thr
XM_017015593.1:c.1075C>A	XP_016871082.1:p.Pro359Thr
XM_017015594.1:c.1024C>A	XP_016871083.1:p.Pro342Thr
XM_024447783.1:c.1186C>A	XP_024303551.1:p.Pro396Thr
XR_001747314.1:n.92+467G>T
NM_001202464.3:c.1075C>A	NP_001189393.1:p.Pro359Thr
NM_001202465.3:c.982C>A	NP_001189394.1:p.Pro328Thr
NM_001202466.3:c.1072C>A	NP_001189395.1:p.Pro358Thr
NM_001330057.3:c.1186C>A	NP_001316986.1:p.Pro396Thr
NM_001370097.3:c.1237C>A	NP_001357026.1:p.Pro413Thr
NM_001370098.2:c.1237C>A	NP_001357027.1:p.Pro413Thr
NM_001370099.2:c.1237C>A	NP_001357028.1:p.Pro413Thr
NM_001370100.4:c.1237C>A	NP_001357029.1:p.Pro413Thr
NM_001370101.2:c.1237C>A	NP_001357030.1:p.Pro413Thr
NM_001370102.2:c.1237C>A	NP_001357031.1:p.Pro413Thr
NM_001370103.2:c.1075C>A	NP_001357032.1:p.Pro359Thr
NM_001370104.2:c.1075C>A	NP_001357033.1:p.Pro359Thr
NM_001370105.2:c.1075C>A	NP_001357034.1:p.Pro359Thr
NM_001370106.2:c.1075C>A	NP_001357035.1:p.Pro359Thr
NM_001370107.2:c.1075C>A	NP_001357036.1:p.Pro359Thr
NM_001370108.2:c.1075C>A	NP_001357037.1:p.Pro359Thr
NM_001370109.2:c.1075C>A	NP_001357038.1:p.Pro359Thr
NM_001370110.2:c.982C>A	NP_001357039.1:p.Pro328Thr
NM_001370111.2:c.1072C>A	NP_001357040.1:p.Pro358Thr
NM_001370112.2:c.1186C>A	NP_001357041.1:p.Pro396Thr
NM_001370113.2:c.1144C>A	NP_001357042.1:p.Pro382Thr
NM_001370114.2:c.1144C>A	NP_001357043.1:p.Pro382Thr
NM_001370115.2:c.1234C>A	NP_001357044.1:p.Pro412Thr
NM_001370116.2:c.1171C>A	NP_001357045.1:p.Pro391Thr
NM_001370117.2:c.1168C>A	NP_001357046.1:p.Pro390Thr
NM_001370118.2:c.1117C>A	NP_001357047.1:p.Pro373Thr
NM_001370119.2:c.1090C>A	NP_001357048.1:p.Pro364Thr
NM_001370120.2:c.1009C>A	NP_001357049.1:p.Pro337Thr
NM_001370121.2:c.955C>A	NP_001357050.1:p.Pro319Thr
NM_001370122.2:c.931C>A	NP_001357051.1:p.Pro311Thr
NM_001370123.2:c.880C>A	NP_001357052.1:p.Pro294Thr
NM_001370124.3:c.766C>A	NP_001357053.1:p.Pro256Thr
NM_006624.7:c.1237C>A	NP_006615.2:p.Pro413Thr
NM_212479.4:c.1234C>A	NP_997644.2:p.Pro412Thr
NR_163254.2:n.1268C>A
NM_001370100.5:c.1237C>A MANE Select	NP_001357029.1:p.Pro413Thr