Canonical Allele Identifier: CA2201615289
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362646T= , CM000678.2:g.1362646T= GRCh38
NC_000016.9:g.1412647T= , CM000678.1:g.1412647T= GRCh37
NC_000016.8:g.1352648T= NCBI36
NG_016985.1:g.15748T=
NG_033129.1:g.57059A=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.744T=
ENST00000529110.2:c.729T= ENSP00000435349.2:p.Asp243=
ENST00000529957.6:n.703T=
ENST00000683366.1:c.*377T= ENSP00000507283.1:n.*377T=
ENST00000683887.1:c.693T= ENSP00000506886.1:p.Asp231=
ENST00000684100.1:n.639T=
ENST00000684126.1:n.779T=
ENST00000684688.1:n.1270T=
ENST00000204679.9:c.645T= MANE Select ENSP00000204679.4:p.Asp215=
ENST00000204679.8:c.645T= ENSP00000204679.4:p.Asp215=
ENST00000527076.1:n.1868T=
ENST00000527168.5:n.812T=
ENST00000529957.5:n.744T=
NM_032520.4:c.645T= NP_115909.1:p.Asp215=
XM_017023782.1:c.693T= XP_016879271.1:p.Asp231=
XM_017023783.1:c.285T= XP_016879272.1:p.Asp95=
NM_032520.5:c.645T= MANE Select NP_115909.1:p.Asp215=