Canonical Allele Identifier: CA7807594
Gene: GNPTG HGNC NCBI

Linked Data

dbSNP Id: rs749320662
gnomAD v2: 16-1411943-A-G
gnomAD v3: 16-1361942-A-G
gnomAD v4: 16-1361942-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1361942A>G , CM000678.2:g.1361942A>G GRCh38
NC_000016.9:g.1411943A>G , CM000678.1:g.1411943A>G GRCh37
NC_000016.8:g.1351944A>G NCBI36
NG_016985.1:g.15044A>G
NG_033129.1:g.57763T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.403A>G
ENST00000529110.2:c.388A>G ENSP00000435349.2:p.Ser130Gly
ENST00000529957.6:n.362A>G
ENST00000683366.1:c.*36A>G ENSP00000507283.1:n.*36A>G
ENST00000683887.1:c.352A>G ENSP00000506886.1:p.Ser118Gly
ENST00000684100.1:n.298A>G
ENST00000684126.1:n.362A>G
ENST00000684688.1:n.929A>G
ENST00000204679.9:c.304A>G MANE Select ENSP00000204679.4:p.Ser102Gly
ENST00000204679.8:c.304A>G ENSP00000204679.4:p.Ser102Gly
ENST00000526820.5:c.*206A>G ENSP00000434413.1:n.*206A>G
ENST00000527076.1:n.1320A>G
ENST00000527168.5:n.340A>G
ENST00000529110.1:c.371A>G
ENST00000529957.5:n.403A>G
NM_032520.4:c.304A>G NP_115909.1:p.Ser102Gly
XM_017023782.1:c.352A>G XP_016879271.1:p.Ser118Gly
XM_017023783.1:c.-57A>G XP_016879272.1:n.-57A>G
NM_032520.5:c.304A>G MANE Select NP_115909.1:p.Ser102Gly