Canonical Allele Identifier: CA359786220

Gene: MAP3K1

Linked Data

• dbSNP Id: rs748188709
• MyVariant Identifiers: chr5:g.56177663G>C (hg19) ; chr5:g.56881836G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881836G>C , CM000667.2:g.56881836G>C	GRCh38
NC_000005.9:g.56177663G>C , CM000667.1:g.56177663G>C	GRCh37
NC_000005.8:g.56213420G>C	NCBI36
NG_031884.1:g.71764G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2636G>C MANE Select	ENSP00000382423.3:p.Gly879Ala
ENST00000399503.3:c.2636G>C	ENSP00000382423.3:p.Gly879Ala
NM_005921.1:c.2636G>C	NP_005912.1:p.Gly879Ala
XM_005248519.3:c.2258G>C	XP_005248576.2:p.Gly753Ala
XM_011543406.1:c.2381G>C	XP_011541708.1:p.Gly794Ala
XM_011543407.1:c.2357G>C	XP_011541709.1:p.Gly786Ala
XM_011543408.1:c.2636G>C	XP_011541710.1:p.Gly879Ala
XM_017009484.1:c.2225G>C	XP_016864973.1:p.Gly742Ala
XM_017009485.1:c.2147G>C	XP_016864974.1:p.Gly716Ala
XR_001742068.2:n.2667G>C
NM_005921.2:c.2636G>C MANE Select	NP_005912.1:p.Gly879Ala