Canonical Allele Identifier: CA2201614181
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1361923C= , CM000678.2:g.1361923C= GRCh38
NC_000016.9:g.1411924C= , CM000678.1:g.1411924C= GRCh37
NC_000016.8:g.1351925C= NCBI36
NG_016985.1:g.15025C=
NG_033129.1:g.57782G=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.384C=
ENST00000529110.2:c.369C= ENSP00000435349.2:p.Thr123=
ENST00000529957.6:n.343C=
ENST00000683366.1:c.*17C= ENSP00000507283.1:n.*17C=
ENST00000683887.1:c.333C= ENSP00000506886.1:p.Thr111=
ENST00000684100.1:n.279C=
ENST00000684126.1:n.343C=
ENST00000684688.1:n.910C=
ENST00000204679.9:c.285C= MANE Select ENSP00000204679.4:p.Thr95=
ENST00000204679.8:c.285C= ENSP00000204679.4:p.Thr95=
ENST00000526820.5:c.*187C= ENSP00000434413.1:n.*187C=
ENST00000527076.1:n.1301C=
ENST00000527168.5:n.321C=
ENST00000529110.1:c.352C=
ENST00000529957.5:n.384C=
NM_032520.4:c.285C= NP_115909.1:p.Thr95=
XM_017023782.1:c.333C= XP_016879271.1:p.Thr111=
XM_017023783.1:c.-76C= XP_016879272.1:n.-76C=
NM_032520.5:c.285C= MANE Select NP_115909.1:p.Thr95=