Canonical Allele Identifier: CA2540316423

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882367_56882368insT , CM000667.2:g.56882367_56882368insT	GRCh38
NC_000005.9:g.56178194_56178195insT , CM000667.1:g.56178194_56178195insT	GRCh37
NC_000005.8:g.56213951_56213952insT	NCBI36
NG_031884.1:g.72295_72296insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3167_3168insT MANE Select	ENSP00000382423.3:p.Ile1057HisfsTer8
ENST00000399503.3:c.3167_3168insT	ENSP00000382423.3:p.Ile1057HisfsTer8
NM_005921.1:c.3167_3168insT	NP_005912.1:p.Ile1057HisfsTer8
XM_005248519.3:c.2789_2790insT	XP_005248576.2:p.Ile931HisfsTer8
XM_011543406.1:c.2912_2913insT	XP_011541708.1:p.Ile972HisfsTer8
XM_011543407.1:c.2888_2889insT	XP_011541709.1:p.Ile964HisfsTer8
XM_011543408.1:c.3167_3168insT	XP_011541710.1:p.Ile1057HisfsTer8
XM_017009484.1:c.2756_2757insT	XP_016864973.1:p.Ile920HisfsTer8
XM_017009485.1:c.2678_2679insT	XP_016864974.1:p.Ile894HisfsTer8
XR_001742068.2:n.3198_3199insT
NM_005921.2:c.3167_3168insT MANE Select	NP_005912.1:p.Ile1057HisfsTer8