Canonical Allele Identifier: CA2201615082

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362369A= , CM000678.2:g.1362369A=	GRCh38
NC_000016.9:g.1412370A= , CM000678.1:g.1412370A=	GRCh37
NC_000016.8:g.1352371A=	NCBI36
NG_016985.1:g.15471A=
NG_033129.1:g.57336T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.625+49A=
ENST00000529110.2:c.610+49A=	ENSP00000435349.2:n.610+49A=
ENST00000529957.6:n.584+49A=
ENST00000683366.1:c.*258+49A=	ENSP00000507283.1:n.*258+49A=
ENST00000683887.1:c.574+49A=	ENSP00000506886.1:n.574+49A=
ENST00000684100.1:n.520+49A=
ENST00000684126.1:n.584+49A=
ENST00000684688.1:n.1151+49A=
ENST00000204679.9:c.526+49A= MANE Select	ENSP00000204679.4:n.526+49A=
ENST00000204679.8:c.526+49A=	ENSP00000204679.4:n.526+49A=
ENST00000527076.1:n.1591A=
ENST00000527168.5:n.611A=
ENST00000529957.5:n.625+49A=
NM_032520.4:c.526+49A=	NP_115909.1:n.526+49A=
XM_017023782.1:c.574+49A=	XP_016879271.1:n.574+49A=
XM_017023783.1:c.166+49A=	XP_016879272.1:n.166+49A=
NM_032520.5:c.526+49A= MANE Select	NP_115909.1:n.526+49A=