Canonical Allele Identifier: CA2630959163

Gene: GNPTG

Linked Data

• gnomAD v4: 16-1361993-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361993G>T , CM000678.2:g.1361993G>T	GRCh38
NC_000016.9:g.1411994G>T , CM000678.1:g.1411994G>T	GRCh37
NC_000016.8:g.1351995G>T	NCBI36
NG_016985.1:g.15095G>T
NG_033129.1:g.57712C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.416+38G>T
ENST00000529110.2:c.401+38G>T	ENSP00000435349.2:n.401+38G>T
ENST00000529957.6:n.375+38G>T
ENST00000683366.1:c.*49+38G>T	ENSP00000507283.1:n.*49+38G>T
ENST00000683887.1:c.365+38G>T	ENSP00000506886.1:n.365+38G>T
ENST00000684100.1:n.311+38G>T
ENST00000684126.1:n.375+38G>T
ENST00000684688.1:n.942+38G>T
ENST00000204679.9:c.317+38G>T MANE Select	ENSP00000204679.4:n.317+38G>T
ENST00000204679.8:c.317+38G>T	ENSP00000204679.4:n.317+38G>T
ENST00000526820.5:c.*219+38G>T	ENSP00000434413.1:n.*219+38G>T
ENST00000527076.1:n.1333+38G>T
ENST00000527168.5:n.353+38G>T
ENST00000529110.1:c.384+38G>T
ENST00000529957.5:n.416+38G>T
NM_032520.4:c.317+38G>T	NP_115909.1:n.317+38G>T
XM_017023782.1:c.365+38G>T	XP_016879271.1:n.365+38G>T
XM_017023783.1:c.-44+38G>T	XP_016879272.1:n.-44+38G>T
NM_032520.5:c.317+38G>T MANE Select	NP_115909.1:n.317+38G>T