Canonical Allele Identifier: CA2201615276
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362633C= , CM000678.2:g.1362633C= GRCh38
NC_000016.9:g.1412634C= , CM000678.1:g.1412634C= GRCh37
NC_000016.8:g.1352635C= NCBI36
NG_016985.1:g.15735C=
NG_033129.1:g.57072G=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.731C=
ENST00000529110.2:c.716C= ENSP00000435349.2:p.Thr239=
ENST00000529957.6:n.690C=
ENST00000683366.1:c.*364C= ENSP00000507283.1:n.*364C=
ENST00000683887.1:c.680C= ENSP00000506886.1:p.Thr227=
ENST00000684100.1:n.626C=
ENST00000684126.1:n.766C=
ENST00000684688.1:n.1257C=
ENST00000204679.9:c.632C= MANE Select ENSP00000204679.4:p.Thr211=
ENST00000204679.8:c.632C= ENSP00000204679.4:p.Thr211=
ENST00000527076.1:n.1855C=
ENST00000527168.5:n.799C=
ENST00000529957.5:n.731C=
NM_032520.4:c.632C= NP_115909.1:p.Thr211=
XM_017023782.1:c.680C= XP_016879271.1:p.Thr227=
XM_017023783.1:c.272C= XP_016879272.1:p.Thr91=
NM_032520.5:c.632C= MANE Select NP_115909.1:p.Thr211=