Canonical Allele Identifier: CA1548139501
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882201G= , CM000667.2:g.56882201G= GRCh38
NC_000005.9:g.56178028G= , CM000667.1:g.56178028G= GRCh37
NC_000005.8:g.56213785G= NCBI36
NG_031884.1:g.72129G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3001G= MANE Select ENSP00000382423.3:p.Val1001=
ENST00000399503.3:c.3001G= ENSP00000382423.3:p.Val1001=
NM_005921.1:c.3001G= NP_005912.1:p.Val1001=
XM_005248519.3:c.2623G= XP_005248576.2:p.Val875=
XM_011543406.1:c.2746G= XP_011541708.1:p.Val916=
XM_011543407.1:c.2722G= XP_011541709.1:p.Val908=
XM_011543408.1:c.3001G= XP_011541710.1:p.Val1001=
XM_017009484.1:c.2590G= XP_016864973.1:p.Val864=
XM_017009485.1:c.2512G= XP_016864974.1:p.Val838=
XR_001742068.2:n.3032G=
NM_005921.2:c.3001G= MANE Select NP_005912.1:p.Val1001=