Canonical Allele Identifier: CA359786061

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177588G>C (hg19) ; chr5:g.56881761G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881761G>C , CM000667.2:g.56881761G>C	GRCh38
NC_000005.9:g.56177588G>C , CM000667.1:g.56177588G>C	GRCh37
NC_000005.8:g.56213345G>C	NCBI36
NG_031884.1:g.71689G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2561G>C MANE Select	ENSP00000382423.3:p.Arg854Pro
ENST00000399503.3:c.2561G>C	ENSP00000382423.3:p.Arg854Pro
NM_005921.1:c.2561G>C	NP_005912.1:p.Arg854Pro
XM_005248519.3:c.2183G>C	XP_005248576.2:p.Arg728Pro
XM_011543406.1:c.2306G>C	XP_011541708.1:p.Arg769Pro
XM_011543407.1:c.2282G>C	XP_011541709.1:p.Arg761Pro
XM_011543408.1:c.2561G>C	XP_011541710.1:p.Arg854Pro
XM_017009484.1:c.2150G>C	XP_016864973.1:p.Arg717Pro
XM_017009485.1:c.2072G>C	XP_016864974.1:p.Arg691Pro
XR_001742068.2:n.2592G>C
NM_005921.2:c.2561G>C MANE Select	NP_005912.1:p.Arg854Pro