Canonical Allele Identifier: CA2081142164

Gene: POMP

Linked Data

• dbSNP Id: rs1884296179

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28659482T>G , CM000675.2:g.28659482T>G	GRCh38
NC_000013.10:g.29233619T>G , CM000675.1:g.29233619T>G	GRCh37
NC_000013.9:g.28131619T>G	NCBI36
NG_027550.1:g.5479T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697661.1:c.-246+295T>G	ENSP00000513386.1:n.-246+295T>G
ENST00000697662.1:c.-282+295T>G	ENSP00000513387.1:n.-282+295T>G
ENST00000697716.1:c.-83+295T>G	ENSP00000513414.1:n.-83+295T>G
ENST00000697717.1:c.3+295T>G	ENSP00000513415.1:n.3+295T>G
ENST00000697718.1:c.3+295T>G	ENSP00000513416.1:n.3+295T>G
ENST00000697719.1:c.-257T>G	ENSP00000513417.1:n.-257T>G
ENST00000697720.1:c.-415T>G	ENSP00000513418.1:n.-415T>G
ENST00000380842.5:c.3+295T>G MANE Select	ENSP00000370222.4:n.3+295T>G
ENST00000380842.4:c.3+295T>G	ENSP00000370222.4:n.3+295T>G
ENST00000460403.1:n.84+295T>G
NM_015932.5:c.3+295T>G	NP_057016.1:n.3+295T>G
XR_941802.1:n.288T>G
NM_015932.6:c.3+295T>G MANE Select	NP_057016.1:n.3+295T>G