Canonical Allele Identifier: CA2201614153
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1361914C= , CM000678.2:g.1361914C= GRCh38
NC_000016.9:g.1411915C= , CM000678.1:g.1411915C= GRCh37
NC_000016.8:g.1351916C= NCBI36
NG_016985.1:g.15016C=
NG_033129.1:g.57791G=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.375C=
ENST00000529110.2:c.360C= ENSP00000435349.2:p.His120=
ENST00000529957.6:n.334C=
ENST00000683366.1:c.*8C= ENSP00000507283.1:n.*8C=
ENST00000683887.1:c.324C= ENSP00000506886.1:p.His108=
ENST00000684100.1:n.270C=
ENST00000684126.1:n.334C=
ENST00000684688.1:n.901C=
ENST00000204679.9:c.276C= MANE Select ENSP00000204679.4:p.His92=
ENST00000204679.8:c.276C= ENSP00000204679.4:p.His92=
ENST00000526820.5:c.*178C= ENSP00000434413.1:n.*178C=
ENST00000527076.1:n.1292C=
ENST00000527168.5:n.312C=
ENST00000529110.1:c.343C=
ENST00000529957.5:n.375C=
NM_032520.4:c.276C= NP_115909.1:p.His92=
XM_017023782.1:c.324C= XP_016879271.1:p.His108=
XM_017023783.1:c.-85C= XP_016879272.1:n.-85C=
NM_032520.5:c.276C= MANE Select NP_115909.1:p.His92=