Canonical Allele Identifier: CA3273110

Gene: MAP3K1

Linked Data

• dbSNP Id: rs374455781
• ExAC: 5:56178095 G / A
• gnomAD v2: 5-56178095-G-A
• gnomAD v3: 5-56882268-G-A
• gnomAD v4: 5-56882268-G-A
• COSMIC: COSM5633998
• MyVariant Identifiers: chr5:g.56178095G>A (hg19) ; chr5:g.56882268G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882268G>A , CM000667.2:g.56882268G>A	GRCh38
NC_000005.9:g.56178095G>A , CM000667.1:g.56178095G>A	GRCh37
NC_000005.8:g.56213852G>A	NCBI36
NG_031884.1:g.72196G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3068G>A MANE Select	ENSP00000382423.3:p.Arg1023His
ENST00000399503.3:c.3068G>A	ENSP00000382423.3:p.Arg1023His
NM_005921.1:c.3068G>A	NP_005912.1:p.Arg1023His
XM_005248519.3:c.2690G>A	XP_005248576.2:p.Arg897His
XM_011543406.1:c.2813G>A	XP_011541708.1:p.Arg938His
XM_011543407.1:c.2789G>A	XP_011541709.1:p.Arg930His
XM_011543408.1:c.3068G>A	XP_011541710.1:p.Arg1023His
XM_017009484.1:c.2657G>A	XP_016864973.1:p.Arg886His
XM_017009485.1:c.2579G>A	XP_016864974.1:p.Arg860His
XR_001742068.2:n.3099G>A
NM_005921.2:c.3068G>A MANE Select	NP_005912.1:p.Arg1023His