Canonical Allele Identifier: CA2201614266

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361954G= , CM000678.2:g.1361954G=	GRCh38
NC_000016.9:g.1411955G= , CM000678.1:g.1411955G=	GRCh37
NC_000016.8:g.1351956G=	NCBI36
NG_016985.1:g.15056G=
NG_033129.1:g.57751C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.415G=
ENST00000529110.2:c.400G=	ENSP00000435349.2:p.Gly134=
ENST00000529957.6:n.374G=
ENST00000683366.1:c.*48G=	ENSP00000507283.1:n.*48G=
ENST00000683887.1:c.364G=	ENSP00000506886.1:p.Gly122=
ENST00000684100.1:n.310G=
ENST00000684126.1:n.374G=
ENST00000684688.1:n.941G=
ENST00000204679.9:c.316G= MANE Select	ENSP00000204679.4:p.Gly106=
ENST00000204679.8:c.316G=	ENSP00000204679.4:p.Gly106=
ENST00000526820.5:c.*218G=	ENSP00000434413.1:n.*218G=
ENST00000527076.1:n.1332G=
ENST00000527168.5:n.352G=
ENST00000529110.1:c.383G=
ENST00000529957.5:n.415G=
NM_032520.4:c.316G=	NP_115909.1:p.Gly106=
XM_017023782.1:c.364G=	XP_016879271.1:p.Gly122=
XM_017023783.1:c.-45G=	XP_016879272.1:n.-45G=
NM_032520.5:c.316G= MANE Select	NP_115909.1:p.Gly106=