Canonical Allele Identifier: CA1548139244
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881631A= , CM000667.2:g.56881631A= GRCh38
NC_000005.9:g.56177458A= , CM000667.1:g.56177458A= GRCh37
NC_000005.8:g.56213215A= NCBI36
NG_031884.1:g.71559A=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.2431A= MANE Select ENSP00000382423.3:p.Met811=
ENST00000399503.3:c.2431A= ENSP00000382423.3:p.Met811=
NM_005921.1:c.2431A= NP_005912.1:p.Met811=
XM_005248519.3:c.2053A= XP_005248576.2:p.Met685=
XM_011543406.1:c.2176A= XP_011541708.1:p.Met726=
XM_011543407.1:c.2152A= XP_011541709.1:p.Met718=
XM_011543408.1:c.2431A= XP_011541710.1:p.Met811=
XM_017009484.1:c.2020A= XP_016864973.1:p.Met674=
XM_017009485.1:c.1942A= XP_016864974.1:p.Met648=
XR_001742068.2:n.2462A=
NM_005921.2:c.2431A= MANE Select NP_005912.1:p.Met811=