Canonical Allele Identifier: CA2843597230

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362573T>C , CM000678.2:g.1362573T>C	GRCh38
NC_000016.9:g.1412574T>C , CM000678.1:g.1412574T>C	GRCh37
NC_000016.8:g.1352575T>C	NCBI36
NG_016985.1:g.15675T>C
NG_033129.1:g.57132A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.709-38T>C
ENST00000529110.2:c.694-38T>C	ENSP00000435349.2:n.694-38T>C
ENST00000529957.6:n.668-38T>C
ENST00000683366.1:c.*342-38T>C	ENSP00000507283.1:n.*342-38T>C
ENST00000683887.1:c.658-38T>C	ENSP00000506886.1:n.658-38T>C
ENST00000684100.1:n.604-38T>C
ENST00000684126.1:n.706T>C
ENST00000684688.1:n.1235-38T>C
ENST00000204679.9:c.610-38T>C MANE Select	ENSP00000204679.4:n.610-38T>C
ENST00000204679.8:c.610-38T>C	ENSP00000204679.4:n.610-38T>C
ENST00000527076.1:n.1795T>C
ENST00000527168.5:n.777-38T>C
ENST00000529957.5:n.709-38T>C
NM_032520.4:c.610-38T>C	NP_115909.1:n.610-38T>C
XM_017023782.1:c.658-38T>C	XP_016879271.1:n.658-38T>C
XM_017023783.1:c.250-38T>C	XP_016879272.1:n.250-38T>C
NM_032520.5:c.610-38T>C MANE Select	NP_115909.1:n.610-38T>C