Canonical Allele Identifier: CA2201615182
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362512C= , CM000678.2:g.1362512C= GRCh38
NC_000016.9:g.1412513C= , CM000678.1:g.1412513C= GRCh37
NC_000016.8:g.1352514C= NCBI36
NG_016985.1:g.15614C=
NG_033129.1:g.57193G=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.686C=
ENST00000529110.2:c.671C= ENSP00000435349.2:p.Ala224=
ENST00000529957.6:n.645C=
ENST00000683366.1:c.*319C= ENSP00000507283.1:n.*319C=
ENST00000683887.1:c.635C= ENSP00000506886.1:p.Ala212=
ENST00000684100.1:n.581C=
ENST00000684126.1:n.645C=
ENST00000684688.1:n.1212C=
ENST00000204679.9:c.587C= MANE Select ENSP00000204679.4:p.Ala196=
ENST00000204679.8:c.587C= ENSP00000204679.4:p.Ala196=
ENST00000527076.1:n.1734C=
ENST00000527168.5:n.754C=
ENST00000529957.5:n.686C=
NM_032520.4:c.587C= NP_115909.1:p.Ala196=
XM_017023782.1:c.635C= XP_016879271.1:p.Ala212=
XM_017023783.1:c.227C= XP_016879272.1:p.Ala76=
NM_032520.5:c.587C= MANE Select NP_115909.1:p.Ala196=