Canonical Allele Identifier: CA2622506760

Gene: POMP

Linked Data

• gnomAD v4: 13-28659208-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28659209del , CM000675.2:g.28659209del	GRCh38
NC_000013.10:g.29233346del , CM000675.1:g.29233346del	GRCh37
NC_000013.9:g.28131346del	NCBI36
NG_027550.1:g.5206del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697661.1:c.-246+22del	ENSP00000513386.1:n.-246+22del
ENST00000697662.1:c.-282+22del	ENSP00000513387.1:n.-282+22del
ENST00000697716.1:c.-83+22del	ENSP00000513414.1:n.-83+22del
ENST00000697717.1:c.3+22del	ENSP00000513415.1:n.3+22del
ENST00000697718.1:c.3+22del	ENSP00000513416.1:n.3+22del
ENST00000380842.5:c.3+22del MANE Select	ENSP00000370222.4:n.3+22del
ENST00000380842.4:c.3+22del	ENSP00000370222.4:n.3+22del
ENST00000460403.1:n.84+22del
NM_015932.5:c.3+22del	NP_057016.1:n.3+22del
XR_941802.1:n.15del
NM_015932.6:c.3+22del MANE Select	NP_057016.1:n.3+22del