Canonical Allele Identifier: CA1548129254
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859882A= , CM000667.2:g.56859882A= GRCh38
NC_000005.9:g.56155709A= , CM000667.1:g.56155709A= GRCh37
NC_000005.8:g.56191466A= NCBI36
NG_031884.1:g.49810A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.801A= MANE Select ENSP00000382423.3:p.Pro267=
ENST00000399503.3:c.801A= ENSP00000382423.3:p.Pro267=
NM_005921.1:c.801A= NP_005912.1:p.Pro267=
XM_005248519.3:c.423A= XP_005248576.2:p.Pro141=
XM_011543406.1:c.546A= XP_011541708.1:p.Pro182=
XM_011543407.1:c.801A= XP_011541709.1:p.Pro267=
XM_011543408.1:c.801A= XP_011541710.1:p.Pro267=
XM_017009484.1:c.390A= XP_016864973.1:p.Pro130=
XM_017009485.1:c.312A= XP_016864974.1:p.Pro104=
XR_001742068.2:n.832A=
NM_005921.2:c.801A= MANE Select NP_005912.1:p.Pro267=