Canonical Allele Identifier: CA2499223211

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1352026C>T , CM000678.2:g.1352026C>T	GRCh38
NC_000016.9:g.1402027C>T , CM000678.1:g.1402027C>T	GRCh37
NC_000016.8:g.1342028C>T	NCBI36
NG_016985.1:g.5128C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_032520.5:c.52+9C>T MANE Select	NP_115909.1:n.52+9C>T
ENST00000204679.9:c.52+9C>T MANE Select	ENSP00000204679.4:n.52+9C>T
NM_032520.4:c.52+9C>T	NP_115909.1:n.52+9C>T
ENST00000204679.8:c.52+9C>T	ENSP00000204679.4:n.52+9C>T
ENST00000526820.5:c.52+9C>T	ENSP00000434413.1:n.52+9C>T
ENST00000527137.2:c.52+9C>T	ENSP00000480060.1:n.52+9C>T
ENST00000527168.5:n.64+9C>T
ENST00000527168.6:n.72+9C>T
ENST00000527876.5:c.52+9C>T	ENSP00000460728.1:n.52+9C>T
ENST00000529110.1:c.44C>T
ENST00000529110.2:c.61C>T	ENSP00000435349.2:p.Pro21Ser
ENST00000529957.5:n.72+9C>T
ENST00000534197.5:n.70+9C>T
ENST00000683366.1:c.52+9C>T	ENSP00000507283.1:n.52+9C>T
ENST00000683887.1:c.52+9C>T	ENSP00000506886.1:n.52+9C>T
XM_017023782.1:c.52+9C>T	XP_016879271.1:n.52+9C>T