Canonical Allele Identifier: CA2261182684

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44007429G= , CM000679.2:g.44007429G= GRCh38
NC_000017.10:g.42084797G= , CM000679.1:g.42084797G= GRCh37
NC_000017.9:g.39440323G= NCBI36
NG_008106.1:g.7766G=
NG_023338.1:g.2041C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.1203G= (NAGS) MANE Select ENSP00000293404.2:p.Lys401=
ENST00000293404.7:c.1203G= (NAGS) ENSP00000293404.2:p.Lys401=
ENST00000589767.1:c.1110G= (NAGS) ENSP00000465408.1:p.Lys370=
ENST00000592915.1:n.1091G= (NAGS)
NM_153006.2:c.1203G= (NAGS) NP_694551.1:p.Lys401=
XM_011524438.1:c.1203G= (NAGS) XP_011522740.1:p.Lys401=
XM_011524439.1:c.705G= (NAGS) XP_011522741.1:p.Lys235=
XM_011525035.1:c.-463+16143C= (PYY) XP_011523337.1:n.-463+16143C=
XM_011524439.2:c.705G= (NAGS) XP_011522741.1:p.Lys235=
NM_153006.3:c.1203G= (NAGS) MANE Select NP_694551.1:p.Lys401=