Canonical Allele Identifier: CA7807952
Gene: GNPTG HGNC NCBI

Linked Data

dbSNP Id: rs779227679
gnomAD v2: 16-1412875-C-A
gnomAD v4: 16-1362874-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362874C>A , CM000678.2:g.1362874C>A GRCh38
NC_000016.9:g.1412875C>A , CM000678.1:g.1412875C>A GRCh37
NC_000016.8:g.1352876C>A NCBI36
NG_016985.1:g.15976C>A
NG_033129.1:g.56831G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000527168.6:n.890C>A
ENST00000529110.2:c.875C>A ENSP00000435349.2:p.Thr292Asn
ENST00000529957.6:n.849C>A
ENST00000683366.1:c.*523C>A ENSP00000507283.1:n.*523C>A
ENST00000683887.1:c.839C>A ENSP00000506886.1:p.Thr280Asn
ENST00000684100.1:n.785C>A
ENST00000684126.1:n.925C>A
ENST00000684688.1:n.1416C>A
ENST00000204679.9:c.791C>A MANE Select ENSP00000204679.4:p.Thr264Asn
ENST00000204679.8:c.791C>A ENSP00000204679.4:p.Thr264Asn
ENST00000527076.1:n.2014C>A
ENST00000527168.5:n.958C>A
ENST00000529957.5:n.890C>A
NM_032520.4:c.791C>A NP_115909.1:p.Thr264Asn
XM_017023782.1:c.839C>A XP_016879271.1:p.Thr280Asn
XM_017023783.1:c.431C>A XP_016879272.1:p.Thr144Asn
NM_032520.5:c.791C>A MANE Select NP_115909.1:p.Thr264Asn