Canonical Allele Identifier: CA645557013
Gene: MAP3K1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881959dup , CM000667.2:g.56881959dup GRCh38
NC_000005.9:g.56177786dup , CM000667.1:g.56177786dup GRCh37
NC_000005.8:g.56213543dup NCBI36
NG_031884.1:g.71887dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2759dup MANE Select ENSP00000382423.3:p.Leu920PhefsTer10
ENST00000399503.3:c.2759dup ENSP00000382423.3:p.Leu920PhefsTer10
NM_005921.1:c.2759dup NP_005912.1:p.Leu920PhefsTer10
XM_005248519.3:c.2381dup XP_005248576.2:p.Leu794PhefsTer10
XM_011543406.1:c.2504dup XP_011541708.1:p.Leu835PhefsTer10
XM_011543407.1:c.2480dup XP_011541709.1:p.Leu827PhefsTer10
XM_011543408.1:c.2759dup XP_011541710.1:p.Leu920PhefsTer10
XM_017009484.1:c.2348dup XP_016864973.1:p.Leu783PhefsTer10
XM_017009485.1:c.2270dup XP_016864974.1:p.Leu757PhefsTer10
XR_001742068.2:n.2790dup
NM_005921.2:c.2759dup MANE Select NP_005912.1:p.Leu920PhefsTer10