Canonical Allele Identifier: CA2201615185
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362516T= , CM000678.2:g.1362516T= GRCh38
NC_000016.9:g.1412517T= , CM000678.1:g.1412517T= GRCh37
NC_000016.8:g.1352518T= NCBI36
NG_016985.1:g.15618T=
NG_033129.1:g.57189A=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.690T=
ENST00000529110.2:c.675T= ENSP00000435349.2:p.Asp225=
ENST00000529957.6:n.649T=
ENST00000683366.1:c.*323T= ENSP00000507283.1:n.*323T=
ENST00000683887.1:c.639T= ENSP00000506886.1:p.Asp213=
ENST00000684100.1:n.585T=
ENST00000684126.1:n.649T=
ENST00000684688.1:n.1216T=
ENST00000204679.9:c.591T= MANE Select ENSP00000204679.4:p.Asp197=
ENST00000204679.8:c.591T= ENSP00000204679.4:p.Asp197=
ENST00000527076.1:n.1738T=
ENST00000527168.5:n.758T=
ENST00000529957.5:n.690T=
NM_032520.4:c.591T= NP_115909.1:p.Asp197=
XM_017023782.1:c.639T= XP_016879271.1:p.Asp213=
XM_017023783.1:c.231T= XP_016879272.1:p.Asp77=
NM_032520.5:c.591T= MANE Select NP_115909.1:p.Asp197=