Canonical Allele Identifier: CA359785845

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177488T>A (hg19) ; chr5:g.56881661T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881661T>A , CM000667.2:g.56881661T>A	GRCh38
NC_000005.9:g.56177488T>A , CM000667.1:g.56177488T>A	GRCh37
NC_000005.8:g.56213245T>A	NCBI36
NG_031884.1:g.71589T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2461T>A MANE Select	ENSP00000382423.3:p.Leu821Met
ENST00000399503.3:c.2461T>A	ENSP00000382423.3:p.Leu821Met
NM_005921.1:c.2461T>A	NP_005912.1:p.Leu821Met
XM_005248519.3:c.2083T>A	XP_005248576.2:p.Leu695Met
XM_011543406.1:c.2206T>A	XP_011541708.1:p.Leu736Met
XM_011543407.1:c.2182T>A	XP_011541709.1:p.Leu728Met
XM_011543408.1:c.2461T>A	XP_011541710.1:p.Leu821Met
XM_017009484.1:c.2050T>A	XP_016864973.1:p.Leu684Met
XM_017009485.1:c.1972T>A	XP_016864974.1:p.Leu658Met
XR_001742068.2:n.2492T>A
NM_005921.2:c.2461T>A MANE Select	NP_005912.1:p.Leu821Met