Canonical Allele Identifier: CA2630961035

Gene: GNPTG

Linked Data

• gnomAD v4: 16-1362579-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362579C>T , CM000678.2:g.1362579C>T	GRCh38
NC_000016.9:g.1412580C>T , CM000678.1:g.1412580C>T	GRCh37
NC_000016.8:g.1352581C>T	NCBI36
NG_016985.1:g.15681C>T
NG_033129.1:g.57126G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.709-32C>T
ENST00000529110.2:c.694-32C>T	ENSP00000435349.2:n.694-32C>T
ENST00000529957.6:n.668-32C>T
ENST00000683366.1:c.*342-32C>T	ENSP00000507283.1:n.*342-32C>T
ENST00000683887.1:c.658-32C>T	ENSP00000506886.1:n.658-32C>T
ENST00000684100.1:n.604-32C>T
ENST00000684126.1:n.712C>T
ENST00000684688.1:n.1235-32C>T
ENST00000204679.9:c.610-32C>T MANE Select	ENSP00000204679.4:n.610-32C>T
ENST00000204679.8:c.610-32C>T	ENSP00000204679.4:n.610-32C>T
ENST00000527076.1:n.1801C>T
ENST00000527168.5:n.777-32C>T
ENST00000529957.5:n.709-32C>T
NM_032520.4:c.610-32C>T	NP_115909.1:n.610-32C>T
XM_017023782.1:c.658-32C>T	XP_016879271.1:n.658-32C>T
XM_017023783.1:c.250-32C>T	XP_016879272.1:n.250-32C>T
NM_032520.5:c.610-32C>T MANE Select	NP_115909.1:n.610-32C>T