Canonical Allele Identifier: CA2201615147
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362452T= , CM000678.2:g.1362452T= GRCh38
NC_000016.9:g.1412453T= , CM000678.1:g.1412453T= GRCh37
NC_000016.8:g.1352454T= NCBI36
NG_016985.1:g.15554T=
NG_033129.1:g.57253A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000527168.6:n.626T=
ENST00000529110.2:c.611T= ENSP00000435349.2:p.Val204=
ENST00000529957.6:n.585T=
ENST00000683366.1:c.*259T= ENSP00000507283.1:n.*259T=
ENST00000683887.1:c.575T= ENSP00000506886.1:p.Val192=
ENST00000684100.1:n.521T=
ENST00000684126.1:n.585T=
ENST00000684688.1:n.1152T=
ENST00000204679.9:c.527T= MANE Select ENSP00000204679.4:p.Val176=
ENST00000204679.8:c.527T= ENSP00000204679.4:p.Val176=
ENST00000527076.1:n.1674T=
ENST00000527168.5:n.694T=
ENST00000529957.5:n.626T=
NM_032520.4:c.527T= NP_115909.1:p.Val176=
XM_017023782.1:c.575T= XP_016879271.1:p.Val192=
XM_017023783.1:c.167T= XP_016879272.1:p.Val56=
NM_032520.5:c.527T= MANE Select NP_115909.1:p.Val176=