Canonical Allele Identifier: CA500616475

Linked Data

MyVariant Identifiers: chr17:g.42085043C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44007675C>G , CM000679.2:g.44007675C>G GRCh38
NC_000017.10:g.42085043C>G , CM000679.1:g.42085043C>G GRCh37
NC_000017.9:g.39440569C>G NCBI36
NG_008106.1:g.8012C>G
NG_023338.1:g.1795G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.1353C>G (NAGS) MANE Select ENSP00000293404.2:p.Arg451=
ENST00000293404.7:c.1353C>G (NAGS) ENSP00000293404.2:p.Arg451=
ENST00000589767.1:c.1284C>G (NAGS) ENSP00000465408.1:p.Arg428=
ENST00000592915.1:n.1241C>G (NAGS)
NM_153006.2:c.1353C>G (NAGS) NP_694551.1:p.Arg451=
XM_011524438.1:c.1268+181C>G (NAGS) XP_011522740.1:n.1268+181C>G
XM_011524439.1:c.855C>G (NAGS) XP_011522741.1:p.Arg285=
XM_011525035.1:c.-463+15897G>C (PYY) XP_011523337.1:n.-463+15897G>C
XM_011524439.2:c.855C>G (NAGS) XP_011522741.1:p.Arg285=
NM_153006.3:c.1353C>G (NAGS) MANE Select NP_694551.1:p.Arg451=