Canonical Allele Identifier: CA2201614232

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1361940A= , CM000678.2:g.1361940A=	GRCh38
NC_000016.9:g.1411941A= , CM000678.1:g.1411941A=	GRCh37
NC_000016.8:g.1351942A=	NCBI36
NG_016985.1:g.15042A=
NG_033129.1:g.57765T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000527168.6:n.401A=
ENST00000529110.2:c.386A=	ENSP00000435349.2:p.Tyr129=
ENST00000529957.6:n.360A=
ENST00000683366.1:c.*34A=	ENSP00000507283.1:n.*34A=
ENST00000683887.1:c.350A=	ENSP00000506886.1:p.Tyr117=
ENST00000684100.1:n.296A=
ENST00000684126.1:n.360A=
ENST00000684688.1:n.927A=
ENST00000204679.9:c.302A= MANE Select	ENSP00000204679.4:p.Tyr101=
ENST00000204679.8:c.302A=	ENSP00000204679.4:p.Tyr101=
ENST00000526820.5:c.*204A=	ENSP00000434413.1:n.*204A=
ENST00000527076.1:n.1318A=
ENST00000527168.5:n.338A=
ENST00000529110.1:c.369A=
ENST00000529957.5:n.401A=
NM_032520.4:c.302A=	NP_115909.1:p.Tyr101=
XM_017023782.1:c.350A=	XP_016879271.1:p.Tyr117=
XM_017023783.1:c.-59A=	XP_016879272.1:n.-59A=
NM_032520.5:c.302A= MANE Select	NP_115909.1:p.Tyr101=