Canonical Allele Identifier: CA399725405

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006071T>G , CM000679.2:g.44006071T>G GRCh38
NC_000017.10:g.42083439T>G , CM000679.1:g.42083439T>G GRCh37
NC_000017.9:g.39438965T>G NCBI36
NG_008106.1:g.6408T>G
NG_023338.1:g.3399A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.749T>G (NAGS) MANE Select ENSP00000293404.2:p.Leu250Arg
ENST00000293404.7:c.749T>G (NAGS) ENSP00000293404.2:p.Leu250Arg
ENST00000589767.1:c.656T>G (NAGS) ENSP00000465408.1:p.Leu219Arg
ENST00000592915.1:n.24T>G (NAGS)
NM_153006.2:c.749T>G (NAGS) NP_694551.1:p.Leu250Arg
XM_011524438.1:c.749T>G (NAGS) XP_011522740.1:p.Leu250Arg
XM_011524439.1:c.251T>G (NAGS) XP_011522741.1:p.Leu84Arg
XM_011525035.1:c.-463+17501A>C (PYY) XP_011523337.1:n.-463+17501A>C
XM_011524439.2:c.251T>G (NAGS) XP_011522741.1:p.Leu84Arg
NM_153006.3:c.749T>G (NAGS) MANE Select NP_694551.1:p.Leu250Arg