Canonical Allele Identifier: CA2201615148
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362456C= , CM000678.2:g.1362456C= GRCh38
NC_000016.9:g.1412457C= , CM000678.1:g.1412457C= GRCh37
NC_000016.8:g.1352458C= NCBI36
NG_016985.1:g.15558C=
NG_033129.1:g.57249G=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.630C=
ENST00000529110.2:c.615C= ENSP00000435349.2:p.Tyr205=
ENST00000529957.6:n.589C=
ENST00000683366.1:c.*263C= ENSP00000507283.1:n.*263C=
ENST00000683887.1:c.579C= ENSP00000506886.1:p.Tyr193=
ENST00000684100.1:n.525C=
ENST00000684126.1:n.589C=
ENST00000684688.1:n.1156C=
ENST00000204679.9:c.531C= MANE Select ENSP00000204679.4:p.Tyr177=
ENST00000204679.8:c.531C= ENSP00000204679.4:p.Tyr177=
ENST00000527076.1:n.1678C=
ENST00000527168.5:n.698C=
ENST00000529957.5:n.630C=
NM_032520.4:c.531C= NP_115909.1:p.Tyr177=
XM_017023782.1:c.579C= XP_016879271.1:p.Tyr193=
XM_017023783.1:c.171C= XP_016879272.1:p.Tyr57=
NM_032520.5:c.531C= MANE Select NP_115909.1:p.Tyr177=