Canonical Allele Identifier: CA1139976208
Gene: REG4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.119809354T= , CM000663.2:g.119809354T= GRCh38
NC_000001.10:g.120351977T= , CM000663.1:g.120351977T= GRCh37
NC_000001.9:g.120153500T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000256585.10:c.-94-491A= MANE Select ENSP00000256585.5:n.-94-491A=
ENST00000256585.9:c.-94-491A= ENSP00000256585.5:n.-94-491A=
ENST00000354219.5:c.-268-152A= ENSP00000346158.1:n.-268-152A=
ENST00000369401.4:c.-94-491A= ENSP00000358409.4:n.-94-491A=
NM_001159352.1:c.-268-152A= NP_001152824.1:n.-268-152A=
NM_001159353.1:c.-94-491A= NP_001152825.1:n.-94-491A=
NM_032044.3:c.-94-491A= NP_114433.1:n.-94-491A=
NM_032044.4:c.-94-491A= MANE Select NP_114433.1:n.-94-491A=
NM_001159352.2:c.-268-152A= NP_001152824.1:n.-268-152A=
NM_001159353.2:c.-94-491A= NP_001152825.1:n.-94-491A=