Canonical Allele Identifier: CA444399036

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177424C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881597C>A , CM000667.2:g.56881597C>A	GRCh38
NC_000005.9:g.56177424C>A , CM000667.1:g.56177424C>A	GRCh37
NC_000005.8:g.56213181C>A	NCBI36
NG_031884.1:g.71525C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2397C>A MANE Select	ENSP00000382423.3:p.Thr799=
ENST00000399503.3:c.2397C>A	ENSP00000382423.3:p.Thr799=
NM_005921.1:c.2397C>A	NP_005912.1:p.Thr799=
XM_005248519.3:c.2019C>A	XP_005248576.2:p.Thr673=
XM_011543406.1:c.2142C>A	XP_011541708.1:p.Thr714=
XM_011543407.1:c.2118C>A	XP_011541709.1:p.Thr706=
XM_011543408.1:c.2397C>A	XP_011541710.1:p.Thr799=
XM_017009484.1:c.1986C>A	XP_016864973.1:p.Thr662=
XM_017009485.1:c.1908C>A	XP_016864974.1:p.Thr636=
XR_001742068.2:n.2428C>A
NM_005921.2:c.2397C>A MANE Select	NP_005912.1:p.Thr799=