Canonical Allele Identifier: CA2261182869

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44007771_44007782delinsCTGGTAGGTCCT , CM000679.2:g.44007771_44007782delinsCTGGTAGGTCCT GRCh38
NC_000017.10:g.42085139_42085150delinsCTGGTAGGTCCT , CM000679.1:g.42085139_42085150delinsCTGGTAGGTCCT GRCh37
NC_000017.9:g.39440665_39440676delinsCTGGTAGGTCCT NCBI36
NG_008106.1:g.8108_8119delinsCTGGTAGGTCCT
NG_023338.1:g.1688_1699delinsAGGACCTACCAG

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.1449_1451+9delinsCTGGTAGGTCCT (NAGS)
ENST00000293404.7:c.1449_1451+9delinsCTGGTAGGTCCT (NAGS)
ENST00000589767.1:c.1380_1382+9delinsCTGGTAGGTCCT (NAGS)
ENST00000592915.1:n.1337_1339+9delinsCTGGTAGGTCCT (NAGS)
NM_153006.2:c.1449_1451+9delinsCTGGTAGGTCCT (NAGS)
XM_011524438.1:c.1268+277_1268+288delinsCTGGTAGGTCCT (NAGS) XP_011522740.1:n.1268+277_1268+288delinsC...
XM_011524439.1:c.951_953+9delinsCTGGTAGGTCCT (NAGS)
XM_011525035.1:c.-463+15790_-463+15801delinsAGGACCTACCAG (PYY) XP_011523337.1:n.-463+15790_-463+15801del...
XM_011524439.2:c.951_953+9delinsCTGGTAGGTCCT (NAGS)
NM_153006.3:c.1449_1451+9delinsCTGGTAGGTCCT (NAGS)