Canonical Allele Identifier: CA2201615269
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362624T= , CM000678.2:g.1362624T= GRCh38
NC_000016.9:g.1412625T= , CM000678.1:g.1412625T= GRCh37
NC_000016.8:g.1352626T= NCBI36
NG_016985.1:g.15726T=
NG_033129.1:g.57081A=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.722T=
ENST00000529110.2:c.707T= ENSP00000435349.2:p.Leu236=
ENST00000529957.6:n.681T=
ENST00000683366.1:c.*355T= ENSP00000507283.1:n.*355T=
ENST00000683887.1:c.671T= ENSP00000506886.1:p.Leu224=
ENST00000684100.1:n.617T=
ENST00000684126.1:n.757T=
ENST00000684688.1:n.1248T=
ENST00000204679.9:c.623T= MANE Select ENSP00000204679.4:p.Leu208=
ENST00000204679.8:c.623T= ENSP00000204679.4:p.Leu208=
ENST00000527076.1:n.1846T=
ENST00000527168.5:n.790T=
ENST00000529957.5:n.722T=
NM_032520.4:c.623T= NP_115909.1:p.Leu208=
XM_017023782.1:c.671T= XP_016879271.1:p.Leu224=
XM_017023783.1:c.263T= XP_016879272.1:p.Leu88=
NM_032520.5:c.623T= MANE Select NP_115909.1:p.Leu208=