Canonical Allele Identifier: CA2201615150
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362458C= , CM000678.2:g.1362458C= GRCh38
NC_000016.9:g.1412459C= , CM000678.1:g.1412459C= GRCh37
NC_000016.8:g.1352460C= NCBI36
NG_016985.1:g.15560C=
NG_033129.1:g.57247G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000527168.6:n.632C=
ENST00000529110.2:c.617C= ENSP00000435349.2:p.Pro206=
ENST00000529957.6:n.591C=
ENST00000683366.1:c.*265C= ENSP00000507283.1:n.*265C=
ENST00000683887.1:c.581C= ENSP00000506886.1:p.Pro194=
ENST00000684100.1:n.527C=
ENST00000684126.1:n.591C=
ENST00000684688.1:n.1158C=
ENST00000204679.9:c.533C= MANE Select ENSP00000204679.4:p.Pro178=
ENST00000204679.8:c.533C= ENSP00000204679.4:p.Pro178=
ENST00000527076.1:n.1680C=
ENST00000527168.5:n.700C=
ENST00000529957.5:n.632C=
NM_032520.4:c.533C= NP_115909.1:p.Pro178=
XM_017023782.1:c.581C= XP_016879271.1:p.Pro194=
XM_017023783.1:c.173C= XP_016879272.1:p.Pro58=
NM_032520.5:c.533C= MANE Select NP_115909.1:p.Pro178=