Canonical Allele Identifier: CA2081141941
Gene: POMP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28659149A= , CM000675.2:g.28659149A= GRCh38
NC_000013.10:g.29233286A= , CM000675.1:g.29233286A= GRCh37
NC_000013.9:g.28131286A= NCBI36
NG_027550.1:g.5146A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697716.1:c.-121A= ENSP00000513414.1:n.-121A=
ENST00000697717.1:c.-36A= ENSP00000513415.1:n.-36A=
ENST00000697718.1:c.-36A= ENSP00000513416.1:n.-36A=
ENST00000380842.5:c.-36A= MANE Select ENSP00000370222.4:n.-36A=
ENST00000380842.4:c.-36A= ENSP00000370222.4:n.-36A=
ENST00000460403.1:n.46A=
NM_015932.5:c.-36A= NP_057016.1:n.-36A=
NM_015932.6:c.-36A= MANE Select NP_057016.1:n.-36A=
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