Canonical Allele Identifier: CA359787635

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178119G>C (hg19) ; chr5:g.56882292G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882292G>C , CM000667.2:g.56882292G>C	GRCh38
NC_000005.9:g.56178119G>C , CM000667.1:g.56178119G>C	GRCh37
NC_000005.8:g.56213876G>C	NCBI36
NG_031884.1:g.72220G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.3092G>C MANE Select	ENSP00000382423.3:p.Arg1031Thr
ENST00000399503.3:c.3092G>C	ENSP00000382423.3:p.Arg1031Thr
NM_005921.1:c.3092G>C	NP_005912.1:p.Arg1031Thr
XM_005248519.3:c.2714G>C	XP_005248576.2:p.Arg905Thr
XM_011543406.1:c.2837G>C	XP_011541708.1:p.Arg946Thr
XM_011543407.1:c.2813G>C	XP_011541709.1:p.Arg938Thr
XM_011543408.1:c.3092G>C	XP_011541710.1:p.Arg1031Thr
XM_017009484.1:c.2681G>C	XP_016864973.1:p.Arg894Thr
XM_017009485.1:c.2603G>C	XP_016864974.1:p.Arg868Thr
XR_001742068.2:n.3123G>C
NM_005921.2:c.3092G>C MANE Select	NP_005912.1:p.Arg1031Thr