Canonical Allele Identifier: CA399725431

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006085A>C , CM000679.2:g.44006085A>C GRCh38
NC_000017.10:g.42083453A>C , CM000679.1:g.42083453A>C GRCh37
NC_000017.9:g.39438979A>C NCBI36
NG_008106.1:g.6422A>C
NG_023338.1:g.3385T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.763A>C (NAGS) MANE Select ENSP00000293404.2:p.Ile255Leu
ENST00000293404.7:c.763A>C (NAGS) ENSP00000293404.2:p.Ile255Leu
ENST00000589767.1:c.670A>C (NAGS) ENSP00000465408.1:p.Ile224Leu
ENST00000592915.1:n.38A>C (NAGS)
NM_153006.2:c.763A>C (NAGS) NP_694551.1:p.Ile255Leu
XM_011524438.1:c.763A>C (NAGS) XP_011522740.1:p.Ile255Leu
XM_011524439.1:c.265A>C (NAGS) XP_011522741.1:p.Ile89Leu
XM_011525035.1:c.-463+17487T>G (PYY) XP_011523337.1:n.-463+17487T>G
XM_011524439.2:c.265A>C (NAGS) XP_011522741.1:p.Ile89Leu
NM_153006.3:c.763A>C (NAGS) MANE Select NP_694551.1:p.Ile255Leu