Canonical Allele Identifier: CA2499224657

Linked Data

ClinVar Variation Id: 1100716
ClinVar RCV Id: RCV001423427

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44007782_44007783delinsCA , CM000679.2:g.44007782_44007783delinsCA GRCh38
NC_000017.10:g.42085150_42085151delinsCA , CM000679.1:g.42085150_42085151delinsCA GRCh37
NC_000017.9:g.39440676_39440677delinsCA NCBI36
NG_008106.1:g.8119_8120delinsCA
NG_023338.1:g.1687_1688delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.1451+9_1451+10delinsCA (NAGS) MANE Select ENSP00000293404.2:n.1451+9_1451+10delinsC...
ENST00000293404.7:c.1451+9_1451+10delinsCA (NAGS) ENSP00000293404.2:n.1451+9_1451+10delinsC...
ENST00000589767.1:c.1382+9_1382+10delinsCA (NAGS) ENSP00000465408.1:n.1382+9_1382+10delinsC...
ENST00000592915.1:n.1339+9_1339+10delinsCA (NAGS)
NM_153006.2:c.1451+9_1451+10delinsCA (NAGS) NP_694551.1:n.1451+9_1451+10delinsCA
XM_011524438.1:c.1268+288_1268+289delinsCA (NAGS) XP_011522740.1:n.1268+288_1268+289delinsC...
XM_011524439.1:c.953+9_953+10delinsCA (NAGS) XP_011522741.1:n.953+9_953+10delinsCA
XM_011525035.1:c.-463+15789_-463+15790delinsTG (PYY) XP_011523337.1:n.-463+15789_-463+15790del...
XM_011524439.2:c.953+9_953+10delinsCA (NAGS) XP_011522741.1:n.953+9_953+10delinsCA
NM_153006.3:c.1451+9_1451+10delinsCA (NAGS) MANE Select NP_694551.1:n.1451+9_1451+10delinsCA