Canonical Allele Identifier: CA359786998

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177919T>A (hg19) ; chr5:g.56882092T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882092T>A , CM000667.2:g.56882092T>A	GRCh38
NC_000005.9:g.56177919T>A , CM000667.1:g.56177919T>A	GRCh37
NC_000005.8:g.56213676T>A	NCBI36
NG_031884.1:g.72020T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2892T>A MANE Select	ENSP00000382423.3:p.Ser964Arg
ENST00000399503.3:c.2892T>A	ENSP00000382423.3:p.Ser964Arg
NM_005921.1:c.2892T>A	NP_005912.1:p.Ser964Arg
XM_005248519.3:c.2514T>A	XP_005248576.2:p.Ser838Arg
XM_011543406.1:c.2637T>A	XP_011541708.1:p.Ser879Arg
XM_011543407.1:c.2613T>A	XP_011541709.1:p.Ser871Arg
XM_011543408.1:c.2892T>A	XP_011541710.1:p.Ser964Arg
XM_017009484.1:c.2481T>A	XP_016864973.1:p.Ser827Arg
XM_017009485.1:c.2403T>A	XP_016864974.1:p.Ser801Arg
XR_001742068.2:n.2923T>A
NM_005921.2:c.2892T>A MANE Select	NP_005912.1:p.Ser964Arg