Canonical Allele Identifier: CA5522627

Gene: MYPN

Linked Data

• ClinVar Variation Id: 477741
• ClinVar RCV Id: RCV000553767 ; RCV002395491
• dbSNP Id: rs745748075
• ExAC: 10:69926059 G / T
• gnomAD v2: 10-69926059-G-T
• gnomAD v3: 10-68166302-G-T
• gnomAD v4: 10-68166302-G-T
• MyVariant Identifiers: chr10:g.69926059G>T (hg19) ; chr10:g.68166302G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166302G>T , CM000672.2:g.68166302G>T	GRCh38
NC_000010.10:g.69926059G>T , CM000672.1:g.69926059G>T	GRCh37
NC_000010.9:g.69596065G>T	NCBI36
NG_032118.1:g.65186G>T , LRG_410:g.65186G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.784G>T	ENSP00000346369.2:p.Asp262Tyr
ENST00000373675.4:c.1609G>T	ENSP00000362779.4:p.Asp537Tyr
ENST00000540630.6:c.1663G>T	ENSP00000441668.3:p.Asp555Tyr
ENST00000613327.5:c.1609G>T	ENSP00000480757.2:p.Asp537Tyr
ENST00000687572.1:c.487G>T	ENSP00000510427.1:p.Asp163Tyr
ENST00000687705.1:c.*1858G>T	ENSP00000509639.1:n.*1858G>T
ENST00000688812.1:c.1585G>T	ENSP00000510658.1:p.Asp529Tyr
ENST00000689002.1:n.661G>T
ENST00000690544.1:c.*880G>T	ENSP00000508989.1:n.*880G>T
ENST00000358913.10:c.1609G>T MANE Select	ENSP00000351790.5:p.Asp537Tyr
ENST00000354393.6:c.784G>T	ENSP00000346369.2:p.Asp262Tyr
ENST00000358913.9:c.1609G>T	ENSP00000351790.5:p.Asp537Tyr
ENST00000540630.5:c.1609G>T	ENSP00000441668.2:p.Asp537Tyr
ENST00000613327.4:c.727G>T	ENSP00000480757.1:p.Asp243Tyr
NM_001256267.1:c.1609G>T	NP_001243196.1:p.Asp537Tyr
NM_001256268.1:c.727G>T	NP_001243197.1:p.Asp243Tyr
NM_032578.3:c.1609G>T , LRG_410t1:c.1609G>T	NP_115967.2:p.Asp537Tyr
NR_045662.3:n.1036G>T
NR_045663.3:n.1877G>T
XM_006718043.2:c.1663G>T	XP_006718106.1:p.Asp555Tyr
XM_011540292.1:c.1639G>T	XP_011538594.1:p.Asp547Tyr
XM_017016833.1:c.1687G>T	XP_016872322.1:p.Asp563Tyr
XM_017016834.2:c.1609G>T	XP_016872323.1:p.Asp537Tyr
XM_024448236.1:c.487G>T	XP_024304004.1:p.Asp163Tyr
NR_045662.4:n.1146G>T
NR_045663.4:n.1822G>T
NM_001256267.2:c.1609G>T	NP_001243196.1:p.Asp537Tyr
NM_001256268.2:c.727G>T	NP_001243197.1:p.Asp243Tyr
NM_032578.4:c.1609G>T MANE Select	NP_115967.2:p.Asp537Tyr