Canonical Allele Identifier: CA654941295
Gene: POMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28659164C>A , CM000675.2:g.28659164C>A GRCh38
NC_000013.10:g.29233301C>A , CM000675.1:g.29233301C>A GRCh37
NC_000013.9:g.28131301C>A NCBI36
NG_027550.1:g.5161C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697716.1:c.-106C>A ENSP00000513414.1:n.-106C>A
ENST00000697717.1:c.-21C>A ENSP00000513415.1:n.-21C>A
ENST00000697718.1:c.-21C>A ENSP00000513416.1:n.-21C>A
ENST00000380842.5:c.-21C>A MANE Select ENSP00000370222.4:n.-21C>A
ENST00000380842.4:c.-21C>A ENSP00000370222.4:n.-21C>A
ENST00000460403.1:n.61C>A
NM_015932.5:c.-21C>A NP_057016.1:n.-21C>A
NM_015932.6:c.-21C>A MANE Select NP_057016.1:n.-21C>A