Canonical Allele Identifier: CA359781272

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56171078T>A (hg19) ; chr5:g.56875251T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875251T>A , CM000667.2:g.56875251T>A	GRCh38
NC_000005.9:g.56171078T>A , CM000667.1:g.56171078T>A	GRCh37
NC_000005.8:g.56206835T>A	NCBI36
NG_031884.1:g.65179T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1906T>A MANE Select	ENSP00000382423.3:p.Cys636Ser
ENST00000399503.3:c.1906T>A	ENSP00000382423.3:p.Cys636Ser
NM_005921.1:c.1906T>A	NP_005912.1:p.Cys636Ser
XM_005248519.3:c.1528T>A	XP_005248576.2:p.Cys510Ser
XM_011543406.1:c.1651T>A	XP_011541708.1:p.Cys551Ser
XM_011543407.1:c.1686+2246T>A	XP_011541709.1:n.1686+2246T>A
XM_011543408.1:c.1906T>A	XP_011541710.1:p.Cys636Ser
XM_017009484.1:c.1495T>A	XP_016864973.1:p.Cys499Ser
XM_017009485.1:c.1417T>A	XP_016864974.1:p.Cys473Ser
XR_001742068.2:n.1937T>A
NM_005921.2:c.1906T>A MANE Select	NP_005912.1:p.Cys636Ser