Canonical Allele Identifier: CA444399513

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178210G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882383G>A , CM000667.2:g.56882383G>A	GRCh38
NC_000005.9:g.56178210G>A , CM000667.1:g.56178210G>A	GRCh37
NC_000005.8:g.56213967G>A	NCBI36
NG_031884.1:g.72311G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3183G>A MANE Select	ENSP00000382423.3:p.Lys1061=
ENST00000399503.3:c.3183G>A	ENSP00000382423.3:p.Lys1061=
NM_005921.1:c.3183G>A	NP_005912.1:p.Lys1061=
XM_005248519.3:c.2805G>A	XP_005248576.2:p.Lys935=
XM_011543406.1:c.2928G>A	XP_011541708.1:p.Lys976=
XM_011543407.1:c.2904G>A	XP_011541709.1:p.Lys968=
XM_011543408.1:c.3183G>A	XP_011541710.1:p.Lys1061=
XM_017009484.1:c.2772G>A	XP_016864973.1:p.Lys924=
XM_017009485.1:c.2694G>A	XP_016864974.1:p.Lys898=
XR_001742068.2:n.3214G>A
NM_005921.2:c.3183G>A MANE Select	NP_005912.1:p.Lys1061=