Canonical Allele Identifier: CA2201615364

Gene: GNPTG

Linked Data

• dbSNP Id: rs2034931912

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362759_1362760insT , CM000678.2:g.1362759_1362760insT	GRCh38
NC_000016.9:g.1412760_1412761insT , CM000678.1:g.1412760_1412761insT	GRCh37
NC_000016.8:g.1352761_1352762insT	NCBI36
NG_016985.1:g.15861_15862insT
NG_033129.1:g.56945_56946insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.840+17_840+18insT
ENST00000529110.2:c.825+17_825+18insT	ENSP00000435349.2:n.825+17_825+18insT
ENST00000529957.6:n.799+17_799+18insT
ENST00000683366.1:c.*473+17_*473+18insT	ENSP00000507283.1:n.*473+17_*473+18insT
ENST00000683887.1:c.789+17_789+18insT	ENSP00000506886.1:n.789+17_789+18insT
ENST00000684100.1:n.735+17_735+18insT
ENST00000684126.1:n.875+17_875+18insT
ENST00000684688.1:n.1366+17_1366+18insT
ENST00000204679.9:c.741+17_741+18insT MANE Select	ENSP00000204679.4:n.741+17_741+18insT
ENST00000204679.8:c.741+17_741+18insT	ENSP00000204679.4:n.741+17_741+18insT
ENST00000527076.1:n.1964+17_1964+18insT
ENST00000527168.5:n.908+17_908+18insT
ENST00000529957.5:n.840+17_840+18insT
NM_032520.4:c.741+17_741+18insT	NP_115909.1:n.741+17_741+18insT
XM_017023782.1:c.789+17_789+18insT	XP_016879271.1:n.789+17_789+18insT
XM_017023783.1:c.381+17_381+18insT	XP_016879272.1:n.381+17_381+18insT
NM_032520.5:c.741+17_741+18insT MANE Select	NP_115909.1:n.741+17_741+18insT