Canonical Allele Identifier: CA444399130

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177541A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881714A>G , CM000667.2:g.56881714A>G	GRCh38
NC_000005.9:g.56177541A>G , CM000667.1:g.56177541A>G	GRCh37
NC_000005.8:g.56213298A>G	NCBI36
NG_031884.1:g.71642A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2514A>G MANE Select	ENSP00000382423.3:p.Leu838=
ENST00000399503.3:c.2514A>G	ENSP00000382423.3:p.Leu838=
NM_005921.1:c.2514A>G	NP_005912.1:p.Leu838=
XM_005248519.3:c.2136A>G	XP_005248576.2:p.Leu712=
XM_011543406.1:c.2259A>G	XP_011541708.1:p.Leu753=
XM_011543407.1:c.2235A>G	XP_011541709.1:p.Leu745=
XM_011543408.1:c.2514A>G	XP_011541710.1:p.Leu838=
XM_017009484.1:c.2103A>G	XP_016864973.1:p.Leu701=
XM_017009485.1:c.2025A>G	XP_016864974.1:p.Leu675=
XR_001742068.2:n.2545A>G
NM_005921.2:c.2514A>G MANE Select	NP_005912.1:p.Leu838=