Canonical Allele Identifier: CA2201614417
Gene: GNPTG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1362022G= , CM000678.2:g.1362022G= GRCh38
NC_000016.9:g.1412023G= , CM000678.1:g.1412023G= GRCh37
NC_000016.8:g.1352024G= NCBI36
NG_016985.1:g.15124G=
NG_033129.1:g.57683C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000527168.6:n.417-16G=
ENST00000529110.2:c.402-16G= ENSP00000435349.2:n.402-16G=
ENST00000529957.6:n.376-16G=
ENST00000683366.1:c.*50-16G= ENSP00000507283.1:n.*50-16G=
ENST00000683887.1:c.366-16G= ENSP00000506886.1:n.366-16G=
ENST00000684100.1:n.312-16G=
ENST00000684126.1:n.376-16G=
ENST00000684688.1:n.943-16G=
ENST00000204679.9:c.318-16G= MANE Select ENSP00000204679.4:n.318-16G=
ENST00000204679.8:c.318-16G= ENSP00000204679.4:n.318-16G=
ENST00000526820.5:c.*220-16G= ENSP00000434413.1:n.*220-16G=
ENST00000527076.1:n.1334-16G=
ENST00000527168.5:n.354-16G=
ENST00000529110.1:c.385-16G=
ENST00000529957.5:n.417-16G=
NM_032520.4:c.318-16G= NP_115909.1:n.318-16G=
XM_017023782.1:c.366-16G= XP_016879271.1:n.366-16G=
XM_017023783.1:c.-43-16G= XP_016879272.1:n.-43-16G=
NM_032520.5:c.318-16G= MANE Select NP_115909.1:n.318-16G=