Canonical Allele Identifier: CA5522666

Gene: MYPN

Linked Data

• ClinVar Variation Id: 1112442
• ClinVar RCV Id: RCV001439405
• dbSNP Id: rs769460067
• ExAC: 10:69926280 A / G
• gnomAD v2: 10-69926280-A-G
• gnomAD v4: 10-68166523-A-G
• MyVariant Identifiers: chr10:g.69926280A>G (hg19) ; chr10:g.68166523A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166523A>G , CM000672.2:g.68166523A>G	GRCh38
NC_000010.10:g.69926280A>G , CM000672.1:g.69926280A>G	GRCh37
NC_000010.9:g.69596286A>G	NCBI36
NG_032118.1:g.65407A>G , LRG_410:g.65407A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1005A>G	ENSP00000346369.2:p.Glu335=
ENST00000373675.4:c.1830A>G	ENSP00000362779.4:p.Glu610=
ENST00000540630.6:c.1884A>G	ENSP00000441668.3:p.Glu628=
ENST00000613327.5:c.1830A>G	ENSP00000480757.2:p.Glu610=
ENST00000687572.1:c.708A>G	ENSP00000510427.1:p.Glu236=
ENST00000688812.1:c.1806A>G	ENSP00000510658.1:p.Glu602=
ENST00000690544.1:c.*1101A>G	ENSP00000508989.1:n.*1101A>G
ENST00000358913.10:c.1830A>G MANE Select	ENSP00000351790.5:p.Glu610=
ENST00000354393.6:c.1005A>G	ENSP00000346369.2:p.Glu335=
ENST00000358913.9:c.1830A>G	ENSP00000351790.5:p.Glu610=
ENST00000540630.5:c.1830A>G	ENSP00000441668.2:p.Glu610=
ENST00000613327.4:c.948A>G	ENSP00000480757.1:p.Glu316=
NM_001256267.1:c.1830A>G	NP_001243196.1:p.Glu610=
NM_001256268.1:c.948A>G	NP_001243197.1:p.Glu316=
NM_032578.3:c.1830A>G , LRG_410t1:c.1830A>G	NP_115967.2:p.Glu610=
NR_045662.3:n.1257A>G
NR_045663.3:n.2098A>G
XM_006718043.2:c.1884A>G	XP_006718106.1:p.Glu628=
XM_011540292.1:c.1860A>G	XP_011538594.1:p.Glu620=
XM_017016833.1:c.1908A>G	XP_016872322.1:p.Glu636=
XM_017016834.2:c.1830A>G	XP_016872323.1:p.Glu610=
XM_024448236.1:c.708A>G	XP_024304004.1:p.Glu236=
NR_045662.4:n.1367A>G
NR_045663.4:n.2043A>G
NM_001256267.2:c.1830A>G	NP_001243196.1:p.Glu610=
NM_001256268.2:c.948A>G	NP_001243197.1:p.Glu316=
NM_032578.4:c.1830A>G MANE Select	NP_115967.2:p.Glu610=