Canonical Allele Identifier: CA500616128

Linked Data

ClinVar Variation Id: 2811213
ClinVar RCV Id: RCV003604191
MyVariant Identifiers: chr17:g.42083533G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006165G>A , CM000679.2:g.44006165G>A GRCh38
NC_000017.10:g.42083533G>A , CM000679.1:g.42083533G>A GRCh37
NC_000017.9:g.39439059G>A NCBI36
NG_008106.1:g.6502G>A
NG_023338.1:g.3305C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.843G>A (NAGS) MANE Select ENSP00000293404.2:p.Leu281=
ENST00000293404.7:c.843G>A (NAGS) ENSP00000293404.2:p.Leu281=
ENST00000589767.1:c.750G>A (NAGS) ENSP00000465408.1:p.Leu250=
ENST00000592915.1:n.118G>A (NAGS)
NM_153006.2:c.843G>A (NAGS) NP_694551.1:p.Leu281=
XM_011524438.1:c.843G>A (NAGS) XP_011522740.1:p.Leu281=
XM_011524439.1:c.345G>A (NAGS) XP_011522741.1:p.Leu115=
XM_011525035.1:c.-463+17407C>T (PYY) XP_011523337.1:n.-463+17407C>T
XM_011524439.2:c.345G>A (NAGS) XP_011522741.1:p.Leu115=
NM_153006.3:c.843G>A (NAGS) MANE Select NP_694551.1:p.Leu281=