Canonical Allele Identifier: CA399727811

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44007685G>C , CM000679.2:g.44007685G>C GRCh38
NC_000017.10:g.42085053G>C , CM000679.1:g.42085053G>C GRCh37
NC_000017.9:g.39440579G>C NCBI36
NG_008106.1:g.8022G>C
NG_023338.1:g.1785C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.1363G>C (NAGS) MANE Select ENSP00000293404.2:p.Gly455Arg
ENST00000293404.7:c.1363G>C (NAGS) ENSP00000293404.2:p.Gly455Arg
ENST00000589767.1:c.1294G>C (NAGS) ENSP00000465408.1:p.Gly432Arg
ENST00000592915.1:n.1251G>C (NAGS)
NM_153006.2:c.1363G>C (NAGS) NP_694551.1:p.Gly455Arg
XM_011524438.1:c.1268+191G>C (NAGS) XP_011522740.1:n.1268+191G>C
XM_011524439.1:c.865G>C (NAGS) XP_011522741.1:p.Gly289Arg
XM_011525035.1:c.-463+15887C>G (PYY) XP_011523337.1:n.-463+15887C>G
XM_011524439.2:c.865G>C (NAGS) XP_011522741.1:p.Gly289Arg
NM_153006.3:c.1363G>C (NAGS) MANE Select NP_694551.1:p.Gly455Arg