Canonical Allele Identifier: CA2839079986

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361811G>C , CM000678.2:g.1361811G>C	GRCh38
NC_000016.9:g.1411812G>C , CM000678.1:g.1411812G>C	GRCh37
NC_000016.8:g.1351813G>C	NCBI36
NG_016985.1:g.14913G>C
NG_033129.1:g.57894C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.332+14G>C
ENST00000529110.2:c.317+14G>C	ENSP00000435349.2:n.317+14G>C
ENST00000529957.6:n.291+14G>C
ENST00000683366.1:c.179-61G>C	ENSP00000507283.1:n.179-61G>C
ENST00000683887.1:c.281+14G>C	ENSP00000506886.1:n.281+14G>C
ENST00000684100.1:n.167G>C
ENST00000684126.1:n.291+14G>C
ENST00000684688.1:n.858+14G>C
ENST00000204679.9:c.233+14G>C MANE Select	ENSP00000204679.4:n.233+14G>C
ENST00000204679.8:c.233+14G>C	ENSP00000204679.4:n.233+14G>C
ENST00000526820.5:c.*135+14G>C	ENSP00000434413.1:n.*135+14G>C
ENST00000527076.1:n.1189G>C
ENST00000527168.5:n.270-61G>C
ENST00000529110.1:c.300+14G>C
ENST00000529957.5:n.332+14G>C
NM_032520.4:c.233+14G>C	NP_115909.1:n.233+14G>C
XM_017023782.1:c.281+14G>C	XP_016879271.1:n.281+14G>C
XM_017023783.1:c.-128+14G>C	XP_016879272.1:n.-128+14G>C
NM_032520.5:c.233+14G>C MANE Select	NP_115909.1:n.233+14G>C