Canonical Allele Identifier: CA2201615265
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362616T= , CM000678.2:g.1362616T= GRCh38
NC_000016.9:g.1412617T= , CM000678.1:g.1412617T= GRCh37
NC_000016.8:g.1352618T= NCBI36
NG_016985.1:g.15718T=
NG_033129.1:g.57089A=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.714T=
ENST00000529110.2:c.699T= ENSP00000435349.2:p.His233=
ENST00000529957.6:n.673T=
ENST00000683366.1:c.*347T= ENSP00000507283.1:n.*347T=
ENST00000683887.1:c.663T= ENSP00000506886.1:p.His221=
ENST00000684100.1:n.609T=
ENST00000684126.1:n.749T=
ENST00000684688.1:n.1240T=
ENST00000204679.9:c.615T= MANE Select ENSP00000204679.4:p.His205=
ENST00000204679.8:c.615T= ENSP00000204679.4:p.His205=
ENST00000527076.1:n.1838T=
ENST00000527168.5:n.782T=
ENST00000529957.5:n.714T=
NM_032520.4:c.615T= NP_115909.1:p.His205=
XM_017023782.1:c.663T= XP_016879271.1:p.His221=
XM_017023783.1:c.255T= XP_016879272.1:p.His85=
NM_032520.5:c.615T= MANE Select NP_115909.1:p.His205=