Canonical Allele Identifier: CA1548139344
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881880C= , CM000667.2:g.56881880C= GRCh38
NC_000005.9:g.56177707C= , CM000667.1:g.56177707C= GRCh37
NC_000005.8:g.56213464C= NCBI36
NG_031884.1:g.71808C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2680C= MANE Select ENSP00000382423.3:p.Leu894=
ENST00000399503.3:c.2680C= ENSP00000382423.3:p.Leu894=
NM_005921.1:c.2680C= NP_005912.1:p.Leu894=
XM_005248519.3:c.2302C= XP_005248576.2:p.Leu768=
XM_011543406.1:c.2425C= XP_011541708.1:p.Leu809=
XM_011543407.1:c.2401C= XP_011541709.1:p.Leu801=
XM_011543408.1:c.2680C= XP_011541710.1:p.Leu894=
XM_017009484.1:c.2269C= XP_016864973.1:p.Leu757=
XM_017009485.1:c.2191C= XP_016864974.1:p.Leu731=
XR_001742068.2:n.2711C=
NM_005921.2:c.2680C= MANE Select NP_005912.1:p.Leu894=