Canonical Allele Identifier: CA2201614013

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361860C= , CM000678.2:g.1361860C=	GRCh38
NC_000016.9:g.1411861C= , CM000678.1:g.1411861C=	GRCh37
NC_000016.8:g.1351862C=	NCBI36
NG_016985.1:g.14962C=
NG_033129.1:g.57845G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.333-12C=
ENST00000529110.2:c.318-12C=	ENSP00000435349.2:n.318-12C=
ENST00000529957.6:n.292-12C=
ENST00000683366.1:c.179-12C=	ENSP00000507283.1:n.179-12C=
ENST00000683887.1:c.282-12C=	ENSP00000506886.1:n.282-12C=
ENST00000684100.1:n.216C=
ENST00000684126.1:n.292-12C=
ENST00000684688.1:n.859-12C=
ENST00000204679.9:c.234-12C= MANE Select	ENSP00000204679.4:n.234-12C=
ENST00000204679.8:c.234-12C=	ENSP00000204679.4:n.234-12C=
ENST00000526820.5:c.*136-12C=	ENSP00000434413.1:n.*136-12C=
ENST00000527076.1:n.1238C=
ENST00000527168.5:n.270-12C=
ENST00000529110.1:c.301-12C=
ENST00000529957.5:n.333-12C=
NM_032520.4:c.234-12C=	NP_115909.1:n.234-12C=
XM_017023782.1:c.282-12C=	XP_016879271.1:n.282-12C=
XM_017023783.1:c.-127-12C=	XP_016879272.1:n.-127-12C=
NM_032520.5:c.234-12C= MANE Select	NP_115909.1:n.234-12C=