Canonical Allele Identifier: CA119079359

Gene: MAP3K1

Linked Data

• dbSNP Id: rs137911818
• gnomAD v3: 5-56881886-A-G
• gnomAD v4: 5-56881886-A-G
• MyVariant Identifiers: chr5:g.56177713A>G (hg19) ; chr5:g.56881886A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881886A>G , CM000667.2:g.56881886A>G	GRCh38
NC_000005.9:g.56177713A>G , CM000667.1:g.56177713A>G	GRCh37
NC_000005.8:g.56213470A>G	NCBI36
NG_031884.1:g.71814A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2686A>G MANE Select	ENSP00000382423.3:p.Thr896Ala
ENST00000399503.3:c.2686A>G	ENSP00000382423.3:p.Thr896Ala
NM_005921.1:c.2686A>G	NP_005912.1:p.Thr896Ala
XM_005248519.3:c.2308A>G	XP_005248576.2:p.Thr770Ala
XM_011543406.1:c.2431A>G	XP_011541708.1:p.Thr811Ala
XM_011543407.1:c.2407A>G	XP_011541709.1:p.Thr803Ala
XM_011543408.1:c.2686A>G	XP_011541710.1:p.Thr896Ala
XM_017009484.1:c.2275A>G	XP_016864973.1:p.Thr759Ala
XM_017009485.1:c.2197A>G	XP_016864974.1:p.Thr733Ala
XR_001742068.2:n.2717A>G
NM_005921.2:c.2686A>G MANE Select	NP_005912.1:p.Thr896Ala