Canonical Allele Identifier: CA697096996

Gene: POMP

Linked Data

• dbSNP Id: rs1444667389
• gnomAD v3: 13-28659400-T-G
• gnomAD v4: 13-28659400-T-G
• MyVariant Identifiers: chr13:g.29233537T>G (hg19) ; chr13:g.28659400T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.28659400T>G , CM000675.2:g.28659400T>G	GRCh38
NC_000013.10:g.29233537T>G , CM000675.1:g.29233537T>G	GRCh37
NC_000013.9:g.28131537T>G	NCBI36
NG_027550.1:g.5397T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697661.1:c.-246+213T>G	ENSP00000513386.1:n.-246+213T>G
ENST00000697662.1:c.-282+213T>G	ENSP00000513387.1:n.-282+213T>G
ENST00000697716.1:c.-83+213T>G	ENSP00000513414.1:n.-83+213T>G
ENST00000697717.1:c.3+213T>G	ENSP00000513415.1:n.3+213T>G
ENST00000697718.1:c.3+213T>G	ENSP00000513416.1:n.3+213T>G
ENST00000697719.1:c.-339T>G	ENSP00000513417.1:n.-339T>G
ENST00000697720.1:c.-497T>G	ENSP00000513418.1:n.-497T>G
ENST00000380842.5:c.3+213T>G MANE Select	ENSP00000370222.4:n.3+213T>G
ENST00000380842.4:c.3+213T>G	ENSP00000370222.4:n.3+213T>G
ENST00000460403.1:n.84+213T>G
NM_015932.5:c.3+213T>G	NP_057016.1:n.3+213T>G
XR_941802.1:n.206T>G
NM_015932.6:c.3+213T>G MANE Select	NP_057016.1:n.3+213T>G