Canonical Allele Identifier: CA444399464

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177910A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882083A>G , CM000667.2:g.56882083A>G	GRCh38
NC_000005.9:g.56177910A>G , CM000667.1:g.56177910A>G	GRCh37
NC_000005.8:g.56213667A>G	NCBI36
NG_031884.1:g.72011A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2883A>G MANE Select	ENSP00000382423.3:p.Arg961=
ENST00000399503.3:c.2883A>G	ENSP00000382423.3:p.Arg961=
NM_005921.1:c.2883A>G	NP_005912.1:p.Arg961=
XM_005248519.3:c.2505A>G	XP_005248576.2:p.Arg835=
XM_011543406.1:c.2628A>G	XP_011541708.1:p.Arg876=
XM_011543407.1:c.2604A>G	XP_011541709.1:p.Arg868=
XM_011543408.1:c.2883A>G	XP_011541710.1:p.Arg961=
XM_017009484.1:c.2472A>G	XP_016864973.1:p.Arg824=
XM_017009485.1:c.2394A>G	XP_016864974.1:p.Arg798=
XR_001742068.2:n.2914A>G
NM_005921.2:c.2883A>G MANE Select	NP_005912.1:p.Arg961=