Canonical Allele Identifier: CA1548129154
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859667A= , CM000667.2:g.56859667A= GRCh38
NC_000005.9:g.56155494A= , CM000667.1:g.56155494A= GRCh37
NC_000005.8:g.56191251A= NCBI36
NG_031884.1:g.49595A=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.634-48A= MANE Select ENSP00000382423.3:n.634-48A=
ENST00000399503.3:c.634-48A= ENSP00000382423.3:n.634-48A=
NM_005921.1:c.634-48A= NP_005912.1:n.634-48A=
XM_005248519.3:c.256-48A= XP_005248576.2:n.256-48A=
XM_011543406.1:c.379-48A= XP_011541708.1:n.379-48A=
XM_011543407.1:c.634-48A= XP_011541709.1:n.634-48A=
XM_011543408.1:c.634-48A= XP_011541710.1:n.634-48A=
XM_017009484.1:c.223-48A= XP_016864973.1:n.223-48A=
XM_017009485.1:c.145-48A= XP_016864974.1:n.145-48A=
XR_001742068.2:n.665-48A=
NM_005921.2:c.634-48A= MANE Select NP_005912.1:n.634-48A=