Canonical Allele Identifier: CA2261182731

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44007525_44007526delinsTG , CM000679.2:g.44007525_44007526delinsTG GRCh38
NC_000017.10:g.42084893_42084894delinsTG , CM000679.1:g.42084893_42084894delinsTG GRCh37
NC_000017.9:g.39440419_39440420delinsTG NCBI36
NG_008106.1:g.7862_7863delinsTG
NG_023338.1:g.1944_1945delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.1268+31_1268+32delinsTG (NAGS) MANE Select ENSP00000293404.2:n.1268+31_1268+32delins...
ENST00000293404.7:c.1268+31_1268+32delinsTG (NAGS) ENSP00000293404.2:n.1268+31_1268+32delins...
ENST00000589767.1:c.1175+31_1175+32delinsTG (NAGS) ENSP00000465408.1:n.1175+31_1175+32delins...
ENST00000592915.1:n.1156+31_1156+32delinsTG (NAGS)
NM_153006.2:c.1268+31_1268+32delinsTG (NAGS) NP_694551.1:n.1268+31_1268+32delinsTG
XM_011524438.1:c.1268+31_1268+32delinsTG (NAGS) XP_011522740.1:n.1268+31_1268+32delinsTG
XM_011524439.1:c.770+31_770+32delinsTG (NAGS) XP_011522741.1:n.770+31_770+32delinsTG
XM_011525035.1:c.-463+16046_-463+16047delinsCA (PYY) XP_011523337.1:n.-463+16046_-463+16047del...
XM_011524439.2:c.770+31_770+32delinsTG (NAGS) XP_011522741.1:n.770+31_770+32delinsTG
NM_153006.3:c.1268+31_1268+32delinsTG (NAGS) MANE Select NP_694551.1:n.1268+31_1268+32delinsTG