Canonical Allele Identifier: CA359781096

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56171040C>A (hg19) ; chr5:g.56875213C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875213C>A , CM000667.2:g.56875213C>A	GRCh38
NC_000005.9:g.56171040C>A , CM000667.1:g.56171040C>A	GRCh37
NC_000005.8:g.56206797C>A	NCBI36
NG_031884.1:g.65141C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1868C>A MANE Select	ENSP00000382423.3:p.Ser623Tyr
ENST00000399503.3:c.1868C>A	ENSP00000382423.3:p.Ser623Tyr
NM_005921.1:c.1868C>A	NP_005912.1:p.Ser623Tyr
XM_005248519.3:c.1490C>A	XP_005248576.2:p.Ser497Tyr
XM_011543406.1:c.1613C>A	XP_011541708.1:p.Ser538Tyr
XM_011543407.1:c.1686+2208C>A	XP_011541709.1:n.1686+2208C>A
XM_011543408.1:c.1868C>A	XP_011541710.1:p.Ser623Tyr
XM_017009484.1:c.1457C>A	XP_016864973.1:p.Ser486Tyr
XM_017009485.1:c.1379C>A	XP_016864974.1:p.Ser460Tyr
XR_001742068.2:n.1899C>A
NM_005921.2:c.1868C>A MANE Select	NP_005912.1:p.Ser623Tyr