Canonical Allele Identifier: CA1548128153
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56857510A= , CM000667.2:g.56857510A= GRCh38
NC_000005.9:g.56153337A= , CM000667.1:g.56153337A= GRCh37
NC_000005.8:g.56189094A= NCBI36
NG_031884.1:g.47438A=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.633+760A= MANE Select ENSP00000382423.3:n.633+760A=
ENST00000399503.3:c.633+760A= ENSP00000382423.3:n.633+760A=
NM_005921.1:c.633+760A= NP_005912.1:n.633+760A=
XM_005248519.3:c.255+760A= XP_005248576.2:n.255+760A=
XM_011543406.1:c.378+760A= XP_011541708.1:n.378+760A=
XM_011543407.1:c.633+760A= XP_011541709.1:n.633+760A=
XM_011543408.1:c.633+760A= XP_011541710.1:n.633+760A=
XM_017009484.1:c.222+760A= XP_016864973.1:n.222+760A=
XM_017009485.1:c.144+760A= XP_016864974.1:n.144+760A=
XR_001742068.2:n.664+760A=
NM_005921.2:c.633+760A= MANE Select NP_005912.1:n.633+760A=