Canonical Allele Identifier: CA2201613700
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1361725G= , CM000678.2:g.1361725G= GRCh38
NC_000016.9:g.1411726G= , CM000678.1:g.1411726G= GRCh37
NC_000016.8:g.1351727G= NCBI36
NG_016985.1:g.14827G=
NG_033129.1:g.57980C=

Transcript Alleles

HGVS Amino-acid change
ENST00000527168.6:n.278-18G=
ENST00000529110.2:c.263-18G= ENSP00000435349.2:n.263-18G=
ENST00000529957.6:n.237-18G=
ENST00000683366.1:c.179-147G= ENSP00000507283.1:n.179-147G=
ENST00000683887.1:c.209G= ENSP00000506886.1:p.Ser70=
ENST00000684100.1:n.81G=
ENST00000684126.1:n.237-18G=
ENST00000684688.1:n.786G=
ENST00000204679.9:c.179-18G= MANE Select ENSP00000204679.4:n.179-18G=
ENST00000204679.8:c.179-18G= ENSP00000204679.4:n.179-18G=
ENST00000526820.5:c.*81-18G= ENSP00000434413.1:n.*81-18G=
ENST00000527076.1:n.1103G=
ENST00000527168.5:n.270-147G=
ENST00000529110.1:c.246-18G=
ENST00000529957.5:n.278-18G=
NM_032520.4:c.179-18G= NP_115909.1:n.179-18G=
XM_017023782.1:c.209G= XP_016879271.1:p.Ser70=
XM_017023783.1:c.-182-18G= XP_016879272.1:n.-182-18G=
NM_032520.5:c.179-18G= MANE Select NP_115909.1:n.179-18G=