Canonical Allele Identifier: CA444399525

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178222T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882395T>A , CM000667.2:g.56882395T>A	GRCh38
NC_000005.9:g.56178222T>A , CM000667.1:g.56178222T>A	GRCh37
NC_000005.8:g.56213979T>A	NCBI36
NG_031884.1:g.72323T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3195T>A MANE Select	ENSP00000382423.3:p.Pro1065=
ENST00000399503.3:c.3195T>A	ENSP00000382423.3:p.Pro1065=
NM_005921.1:c.3195T>A	NP_005912.1:p.Pro1065=
XM_005248519.3:c.2817T>A	XP_005248576.2:p.Pro939=
XM_011543406.1:c.2940T>A	XP_011541708.1:p.Pro980=
XM_011543407.1:c.2916T>A	XP_011541709.1:p.Pro972=
XM_011543408.1:c.3195T>A	XP_011541710.1:p.Pro1065=
XM_017009484.1:c.2784T>A	XP_016864973.1:p.Pro928=
XM_017009485.1:c.2706T>A	XP_016864974.1:p.Pro902=
XR_001742068.2:n.3226T>A
NM_005921.2:c.3195T>A MANE Select	NP_005912.1:p.Pro1065=