Canonical Allele Identifier: CA7807739
Gene: GNPTG HGNC NCBI

Linked Data

dbSNP Id: rs764053747
gnomAD v2: 16-1412294-C-A
gnomAD v4: 16-1362293-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362293C>A , CM000678.2:g.1362293C>A GRCh38
NC_000016.9:g.1412294C>A , CM000678.1:g.1412294C>A GRCh37
NC_000016.8:g.1352295C>A NCBI36
NG_016985.1:g.15395C>A
NG_033129.1:g.57412G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000527168.6:n.598C>A
ENST00000529110.2:c.583C>A ENSP00000435349.2:p.Leu195Ile
ENST00000529957.6:n.557C>A
ENST00000683366.1:c.*231C>A ENSP00000507283.1:n.*231C>A
ENST00000683887.1:c.547C>A ENSP00000506886.1:p.Leu183Ile
ENST00000684100.1:n.493C>A
ENST00000684126.1:n.557C>A
ENST00000684688.1:n.1124C>A
ENST00000204679.9:c.499C>A MANE Select ENSP00000204679.4:p.Leu167Ile
ENST00000204679.8:c.499C>A ENSP00000204679.4:p.Leu167Ile
ENST00000527076.1:n.1515C>A
ENST00000527168.5:n.535C>A
ENST00000529957.5:n.598C>A
NM_032520.4:c.499C>A NP_115909.1:p.Leu167Ile
XM_017023782.1:c.547C>A XP_016879271.1:p.Leu183Ile
XM_017023783.1:c.139C>A XP_016879272.1:p.Leu47Ile
NM_032520.5:c.499C>A MANE Select NP_115909.1:p.Leu167Ile