Canonical Allele Identifier: CA500616126

Linked Data

ClinVar Variation Id: 2738974
ClinVar RCV Id: RCV003497440
dbSNP Id: rs202173320

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006162G>T , CM000679.2:g.44006162G>T GRCh38
NC_000017.10:g.42083530G>T , CM000679.1:g.42083530G>T GRCh37
NC_000017.9:g.39439056G>T NCBI36
NG_008106.1:g.6499G>T
NG_023338.1:g.3308C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.840G>T (NAGS) MANE Select ENSP00000293404.2:p.Ser280=
ENST00000293404.7:c.840G>T (NAGS) ENSP00000293404.2:p.Ser280=
ENST00000589767.1:c.747G>T (NAGS) ENSP00000465408.1:p.Ser249=
ENST00000592915.1:n.115G>T (NAGS)
NM_153006.2:c.840G>T (NAGS) NP_694551.1:p.Ser280=
XM_011524438.1:c.840G>T (NAGS) XP_011522740.1:p.Ser280=
XM_011524439.1:c.342G>T (NAGS) XP_011522741.1:p.Ser114=
XM_011525035.1:c.-463+17410C>A (PYY) XP_011523337.1:n.-463+17410C>A
XM_011524439.2:c.342G>T (NAGS) XP_011522741.1:p.Ser114=
NM_153006.3:c.840G>T (NAGS) MANE Select NP_694551.1:p.Ser280=