Canonical Allele Identifier: CA2201615188
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362521T= , CM000678.2:g.1362521T= GRCh38
NC_000016.9:g.1412522T= , CM000678.1:g.1412522T= GRCh37
NC_000016.8:g.1352523T= NCBI36
NG_016985.1:g.15623T=
NG_033129.1:g.57184A=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.695T=
ENST00000529110.2:c.680T= ENSP00000435349.2:p.Leu227=
ENST00000529957.6:n.654T=
ENST00000683366.1:c.*328T= ENSP00000507283.1:n.*328T=
ENST00000683887.1:c.644T= ENSP00000506886.1:p.Leu215=
ENST00000684100.1:n.590T=
ENST00000684126.1:n.654T=
ENST00000684688.1:n.1221T=
ENST00000204679.9:c.596T= MANE Select ENSP00000204679.4:p.Leu199=
ENST00000204679.8:c.596T= ENSP00000204679.4:p.Leu199=
ENST00000527076.1:n.1743T=
ENST00000527168.5:n.763T=
ENST00000529957.5:n.695T=
NM_032520.4:c.596T= NP_115909.1:p.Leu199=
XM_017023782.1:c.644T= XP_016879271.1:p.Leu215=
XM_017023783.1:c.236T= XP_016879272.1:p.Leu79=
NM_032520.5:c.596T= MANE Select NP_115909.1:p.Leu199=