Canonical Allele Identifier: CA444399432

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178018T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882191T>G , CM000667.2:g.56882191T>G	GRCh38
NC_000005.9:g.56178018T>G , CM000667.1:g.56178018T>G	GRCh37
NC_000005.8:g.56213775T>G	NCBI36
NG_031884.1:g.72119T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.2991T>G MANE Select	ENSP00000382423.3:p.Thr997=
ENST00000399503.3:c.2991T>G	ENSP00000382423.3:p.Thr997=
NM_005921.1:c.2991T>G	NP_005912.1:p.Thr997=
XM_005248519.3:c.2613T>G	XP_005248576.2:p.Thr871=
XM_011543406.1:c.2736T>G	XP_011541708.1:p.Thr912=
XM_011543407.1:c.2712T>G	XP_011541709.1:p.Thr904=
XM_011543408.1:c.2991T>G	XP_011541710.1:p.Thr997=
XM_017009484.1:c.2580T>G	XP_016864973.1:p.Thr860=
XM_017009485.1:c.2502T>G	XP_016864974.1:p.Thr834=
XR_001742068.2:n.3022T>G
NM_005921.2:c.2991T>G MANE Select	NP_005912.1:p.Thr997=