Canonical Allele Identifier: CA399725692

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006164T>A , CM000679.2:g.44006164T>A GRCh38
NC_000017.10:g.42083532T>A , CM000679.1:g.42083532T>A GRCh37
NC_000017.9:g.39439058T>A NCBI36
NG_008106.1:g.6501T>A
NG_023338.1:g.3306A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.842T>A (NAGS) MANE Select ENSP00000293404.2:p.Leu281Gln
ENST00000293404.7:c.842T>A (NAGS) ENSP00000293404.2:p.Leu281Gln
ENST00000589767.1:c.749T>A (NAGS) ENSP00000465408.1:p.Leu250Gln
ENST00000592915.1:n.117T>A (NAGS)
NM_153006.2:c.842T>A (NAGS) NP_694551.1:p.Leu281Gln
XM_011524438.1:c.842T>A (NAGS) XP_011522740.1:p.Leu281Gln
XM_011524439.1:c.344T>A (NAGS) XP_011522741.1:p.Leu115Gln
XM_011525035.1:c.-463+17408A>T (PYY) XP_011523337.1:n.-463+17408A>T
XM_011524439.2:c.344T>A (NAGS) XP_011522741.1:p.Leu115Gln
NM_153006.3:c.842T>A (NAGS) MANE Select NP_694551.1:p.Leu281Gln