Canonical Allele Identifier: CA2638146792

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006415del , CM000679.2:g.44006415del GRCh38
NC_000017.10:g.42083783del , CM000679.1:g.42083783del GRCh37
NC_000017.9:g.39439309del NCBI36
NG_008106.1:g.6752del
NG_023338.1:g.3056del

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.916-114del (NAGS) MANE Select ENSP00000293404.2:n.916-114del
ENST00000293404.7:c.916-114del (NAGS) ENSP00000293404.2:n.916-114del
ENST00000589767.1:c.823-114del (NAGS) ENSP00000465408.1:n.823-114del
ENST00000592915.1:n.191-114del (NAGS)
NM_153006.2:c.916-114del (NAGS) NP_694551.1:n.916-114del
XM_011524438.1:c.916-114del (NAGS) XP_011522740.1:n.916-114del
XM_011524439.1:c.418-114del (NAGS) XP_011522741.1:n.418-114del
XM_011525035.1:c.-463+17158del (PYY) XP_011523337.1:n.-463+17158del
XM_011524439.2:c.418-114del (NAGS) XP_011522741.1:n.418-114del
NM_153006.3:c.916-114del (NAGS) MANE Select NP_694551.1:n.916-114del