Canonical Allele Identifier: CA2622506838

Gene: POMP

Linked Data

• gnomAD v4: 13-28659290-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28659290C>T , CM000675.2:g.28659290C>T	GRCh38
NC_000013.10:g.29233427C>T , CM000675.1:g.29233427C>T	GRCh37
NC_000013.9:g.28131427C>T	NCBI36
NG_027550.1:g.5287C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697661.1:c.-246+103C>T	ENSP00000513386.1:n.-246+103C>T
ENST00000697662.1:c.-282+103C>T	ENSP00000513387.1:n.-282+103C>T
ENST00000697716.1:c.-83+103C>T	ENSP00000513414.1:n.-83+103C>T
ENST00000697717.1:c.3+103C>T	ENSP00000513415.1:n.3+103C>T
ENST00000697718.1:c.3+103C>T	ENSP00000513416.1:n.3+103C>T
ENST00000380842.5:c.3+103C>T MANE Select	ENSP00000370222.4:n.3+103C>T
ENST00000380842.4:c.3+103C>T	ENSP00000370222.4:n.3+103C>T
ENST00000460403.1:n.84+103C>T
NM_015932.5:c.3+103C>T	NP_057016.1:n.3+103C>T
XR_941802.1:n.96C>T
NM_015932.6:c.3+103C>T MANE Select	NP_057016.1:n.3+103C>T