Canonical Allele Identifier: CA444391772

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56155724A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859897A>G , CM000667.2:g.56859897A>G	GRCh38
NC_000005.9:g.56155724A>G , CM000667.1:g.56155724A>G	GRCh37
NC_000005.8:g.56191481A>G	NCBI36
NG_031884.1:g.49825A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.816A>G MANE Select	ENSP00000382423.3:p.Lys272=
ENST00000399503.3:c.816A>G	ENSP00000382423.3:p.Lys272=
NM_005921.1:c.816A>G	NP_005912.1:p.Lys272=
XM_005248519.3:c.438A>G	XP_005248576.2:p.Lys146=
XM_011543406.1:c.561A>G	XP_011541708.1:p.Lys187=
XM_011543407.1:c.816A>G	XP_011541709.1:p.Lys272=
XM_011543408.1:c.816A>G	XP_011541710.1:p.Lys272=
XM_017009484.1:c.405A>G	XP_016864973.1:p.Lys135=
XM_017009485.1:c.327A>G	XP_016864974.1:p.Lys109=
XR_001742068.2:n.847A>G
NM_005921.2:c.816A>G MANE Select	NP_005912.1:p.Lys272=