Canonical Allele Identifier: CA609145026

Gene: POMP

Linked Data

• dbSNP Id: rs1405039573
• gnomAD v2: 13-29233599-C-A
• gnomAD v3: 13-28659462-C-A
• gnomAD v4: 13-28659462-C-A
• MyVariant Identifiers: chr13:g.29233599C>A (hg19) ; chr13:g.28659462C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28659462C>A , CM000675.2:g.28659462C>A	GRCh38
NC_000013.10:g.29233599C>A , CM000675.1:g.29233599C>A	GRCh37
NC_000013.9:g.28131599C>A	NCBI36
NG_027550.1:g.5459C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697661.1:c.-246+275C>A	ENSP00000513386.1:n.-246+275C>A
ENST00000697662.1:c.-282+275C>A	ENSP00000513387.1:n.-282+275C>A
ENST00000697716.1:c.-83+275C>A	ENSP00000513414.1:n.-83+275C>A
ENST00000697717.1:c.3+275C>A	ENSP00000513415.1:n.3+275C>A
ENST00000697718.1:c.3+275C>A	ENSP00000513416.1:n.3+275C>A
ENST00000697719.1:c.-277C>A	ENSP00000513417.1:n.-277C>A
ENST00000697720.1:c.-435C>A	ENSP00000513418.1:n.-435C>A
ENST00000380842.5:c.3+275C>A MANE Select	ENSP00000370222.4:n.3+275C>A
ENST00000380842.4:c.3+275C>A	ENSP00000370222.4:n.3+275C>A
ENST00000460403.1:n.84+275C>A
NM_015932.5:c.3+275C>A	NP_057016.1:n.3+275C>A
XR_941802.1:n.268C>A
NM_015932.6:c.3+275C>A MANE Select	NP_057016.1:n.3+275C>A