Canonical Allele Identifier: CA444399155

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56177586T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881759T>A , CM000667.2:g.56881759T>A	GRCh38
NC_000005.9:g.56177586T>A , CM000667.1:g.56177586T>A	GRCh37
NC_000005.8:g.56213343T>A	NCBI36
NG_031884.1:g.71687T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2559T>A MANE Select	ENSP00000382423.3:p.Arg853=
ENST00000399503.3:c.2559T>A	ENSP00000382423.3:p.Arg853=
NM_005921.1:c.2559T>A	NP_005912.1:p.Arg853=
XM_005248519.3:c.2181T>A	XP_005248576.2:p.Arg727=
XM_011543406.1:c.2304T>A	XP_011541708.1:p.Arg768=
XM_011543407.1:c.2280T>A	XP_011541709.1:p.Arg760=
XM_011543408.1:c.2559T>A	XP_011541710.1:p.Arg853=
XM_017009484.1:c.2148T>A	XP_016864973.1:p.Arg716=
XM_017009485.1:c.2070T>A	XP_016864974.1:p.Arg690=
XR_001742068.2:n.2590T>A
NM_005921.2:c.2559T>A MANE Select	NP_005912.1:p.Arg853=