Canonical Allele Identifier: CA2201613697
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1361723C= , CM000678.2:g.1361723C= GRCh38
NC_000016.9:g.1411724C= , CM000678.1:g.1411724C= GRCh37
NC_000016.8:g.1351725C= NCBI36
NG_016985.1:g.14825C=
NG_033129.1:g.57982G=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.278-20C=
ENST00000529110.2:c.263-20C= ENSP00000435349.2:n.263-20C=
ENST00000529957.6:n.237-20C=
ENST00000683366.1:c.179-149C= ENSP00000507283.1:n.179-149C=
ENST00000683887.1:c.207C= ENSP00000506886.1:p.Ile69=
ENST00000684100.1:n.79C=
ENST00000684126.1:n.237-20C=
ENST00000684688.1:n.784C=
ENST00000204679.9:c.179-20C= MANE Select ENSP00000204679.4:n.179-20C=
ENST00000204679.8:c.179-20C= ENSP00000204679.4:n.179-20C=
ENST00000526820.5:c.*81-20C= ENSP00000434413.1:n.*81-20C=
ENST00000527076.1:n.1101C=
ENST00000527168.5:n.270-149C=
ENST00000529110.1:c.246-20C=
ENST00000529957.5:n.278-20C=
NM_032520.4:c.179-20C= NP_115909.1:n.179-20C=
XM_017023782.1:c.207C= XP_016879271.1:p.Ile69=
XM_017023783.1:c.-182-20C= XP_016879272.1:n.-182-20C=
NM_032520.5:c.179-20C= MANE Select NP_115909.1:n.179-20C=