Canonical Allele Identifier: CA359787697

Gene: MAP3K1

Linked Data

• MyVariant Identifiers: chr5:g.56178145G>T (hg19) ; chr5:g.56882318G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882318G>T , CM000667.2:g.56882318G>T	GRCh38
NC_000005.9:g.56178145G>T , CM000667.1:g.56178145G>T	GRCh37
NC_000005.8:g.56213902G>T	NCBI36
NG_031884.1:g.72246G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3118G>T MANE Select	ENSP00000382423.3:p.Asp1040Tyr
ENST00000399503.3:c.3118G>T	ENSP00000382423.3:p.Asp1040Tyr
NM_005921.1:c.3118G>T	NP_005912.1:p.Asp1040Tyr
XM_005248519.3:c.2740G>T	XP_005248576.2:p.Asp914Tyr
XM_011543406.1:c.2863G>T	XP_011541708.1:p.Asp955Tyr
XM_011543407.1:c.2839G>T	XP_011541709.1:p.Asp947Tyr
XM_011543408.1:c.3118G>T	XP_011541710.1:p.Asp1040Tyr
XM_017009484.1:c.2707G>T	XP_016864973.1:p.Asp903Tyr
XM_017009485.1:c.2629G>T	XP_016864974.1:p.Asp877Tyr
XR_001742068.2:n.3149G>T
NM_005921.2:c.3118G>T MANE Select	NP_005912.1:p.Asp1040Tyr