Canonical Allele Identifier: CA2201615271
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362626C= , CM000678.2:g.1362626C= GRCh38
NC_000016.9:g.1412627C= , CM000678.1:g.1412627C= GRCh37
NC_000016.8:g.1352628C= NCBI36
NG_016985.1:g.15728C=
NG_033129.1:g.57079G=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.724C=
ENST00000529110.2:c.709C= ENSP00000435349.2:p.Leu237=
ENST00000529957.6:n.683C=
ENST00000683366.1:c.*357C= ENSP00000507283.1:n.*357C=
ENST00000683887.1:c.673C= ENSP00000506886.1:p.Leu225=
ENST00000684100.1:n.619C=
ENST00000684126.1:n.759C=
ENST00000684688.1:n.1250C=
ENST00000204679.9:c.625C= MANE Select ENSP00000204679.4:p.Leu209=
ENST00000204679.8:c.625C= ENSP00000204679.4:p.Leu209=
ENST00000527076.1:n.1848C=
ENST00000527168.5:n.792C=
ENST00000529957.5:n.724C=
NM_032520.4:c.625C= NP_115909.1:p.Leu209=
XM_017023782.1:c.673C= XP_016879271.1:p.Leu225=
XM_017023783.1:c.265C= XP_016879272.1:p.Leu89=
NM_032520.5:c.625C= MANE Select NP_115909.1:p.Leu209=