Canonical Allele Identifier: CA1548139411
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882031_56882032delinsCA , CM000667.2:g.56882031_56882032delinsCA GRCh38
NC_000005.9:g.56177858_56177859delinsCA , CM000667.1:g.56177858_56177859delinsCA GRCh37
NC_000005.8:g.56213615_56213616delinsCA NCBI36
NG_031884.1:g.71959_71960delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2831_2832delinsCA MANE Select ENSP00000382423.3:p.Thr944=
ENST00000399503.3:c.2831_2832delinsCA ENSP00000382423.3:p.Thr944=
NM_005921.1:c.2831_2832delinsCA NP_005912.1:p.Thr944=
XM_005248519.3:c.2453_2454delinsCA XP_005248576.2:p.Thr818=
XM_011543406.1:c.2576_2577delinsCA XP_011541708.1:p.Thr859=
XM_011543407.1:c.2552_2553delinsCA XP_011541709.1:p.Thr851=
XM_011543408.1:c.2831_2832delinsCA XP_011541710.1:p.Thr944=
XM_017009484.1:c.2420_2421delinsCA XP_016864973.1:p.Thr807=
XM_017009485.1:c.2342_2343delinsCA XP_016864974.1:p.Thr781=
XR_001742068.2:n.2862_2863delinsCA
NM_005921.2:c.2831_2832delinsCA MANE Select NP_005912.1:p.Thr944=