Canonical Allele Identifier: CA2201615133

Gene: GNPTG

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1362432_1362470delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA , CM000678.2:g.1362432_1362470delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA	GRCh38
NC_000016.9:g.1412433_1412471delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA , CM000678.1:g.1412433_1412471delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA	GRCh37
NC_000016.8:g.1352434_1352472delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA	NCBI36
NG_016985.1:g.15534_15572delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
NG_033129.1:g.57235_57273delinsTCTGGCAGGGTTGGGTACACTGAGGACCCAAGAGAAGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527168.6:n.626-20_644delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
ENST00000529110.2:c.611-20_629delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
ENST00000529957.6:n.585-20_603delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
ENST00000683366.1:c.*259-20_*277delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
ENST00000683887.1:c.575-20_593delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
ENST00000684100.1:n.521-20_539delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
ENST00000684126.1:n.585-20_603delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
ENST00000684688.1:n.1152-20_1170delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
ENST00000204679.9:c.527-20_545delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
ENST00000204679.8:c.527-20_545delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
ENST00000527076.1:n.1654_1692delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
ENST00000527168.5:n.674_712delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
ENST00000529957.5:n.626-20_644delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
NM_032520.4:c.527-20_545delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
XM_017023782.1:c.575-20_593delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
XM_017023783.1:c.167-20_185delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA
NM_032520.5:c.527-20_545delinsGGCTTCTCTTGGGTCCTCAGTGTACCCAACCCTGCCAGA