Canonical Allele Identifier: CA500616127

Linked Data

MyVariant Identifiers: chr17:g.42083531C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006163C>T , CM000679.2:g.44006163C>T GRCh38
NC_000017.10:g.42083531C>T , CM000679.1:g.42083531C>T GRCh37
NC_000017.9:g.39439057C>T NCBI36
NG_008106.1:g.6500C>T
NG_023338.1:g.3307G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.841C>T (NAGS) MANE Select ENSP00000293404.2:p.Leu281=
ENST00000293404.7:c.841C>T (NAGS) ENSP00000293404.2:p.Leu281=
ENST00000589767.1:c.748C>T (NAGS) ENSP00000465408.1:p.Leu250=
ENST00000592915.1:n.116C>T (NAGS)
NM_153006.2:c.841C>T (NAGS) NP_694551.1:p.Leu281=
XM_011524438.1:c.841C>T (NAGS) XP_011522740.1:p.Leu281=
XM_011524439.1:c.343C>T (NAGS) XP_011522741.1:p.Leu115=
XM_011525035.1:c.-463+17409G>A (PYY) XP_011523337.1:n.-463+17409G>A
XM_011524439.2:c.343C>T (NAGS) XP_011522741.1:p.Leu115=
NM_153006.3:c.841C>T (NAGS) MANE Select NP_694551.1:p.Leu281=