Canonical Allele Identifier: CA2731773744

Gene: GNPTG

Linked Data

• dbSNP Id: rs2141864730

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362781T>C , CM000678.2:g.1362781T>C	GRCh38
NC_000016.9:g.1412782T>C , CM000678.1:g.1412782T>C	GRCh37
NC_000016.8:g.1352783T>C	NCBI36
NG_016985.1:g.15883T>C
NG_033129.1:g.56924A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.840+39T>C
ENST00000529110.2:c.825+39T>C	ENSP00000435349.2:n.825+39T>C
ENST00000529957.6:n.799+39T>C
ENST00000683366.1:c.*473+39T>C	ENSP00000507283.1:n.*473+39T>C
ENST00000683887.1:c.789+39T>C	ENSP00000506886.1:n.789+39T>C
ENST00000684100.1:n.735+39T>C
ENST00000684126.1:n.875+39T>C
ENST00000684688.1:n.1366+39T>C
ENST00000204679.9:c.741+39T>C MANE Select	ENSP00000204679.4:n.741+39T>C
ENST00000204679.8:c.741+39T>C	ENSP00000204679.4:n.741+39T>C
ENST00000527076.1:n.1964+39T>C
ENST00000527168.5:n.908+39T>C
ENST00000529957.5:n.840+39T>C
NM_032520.4:c.741+39T>C	NP_115909.1:n.741+39T>C
XM_017023782.1:c.789+39T>C	XP_016879271.1:n.789+39T>C
XM_017023783.1:c.381+39T>C	XP_016879272.1:n.381+39T>C
NM_032520.5:c.741+39T>C MANE Select	NP_115909.1:n.741+39T>C