Canonical Allele Identifier: CA2261182683

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44007428A= , CM000679.2:g.44007428A= GRCh38
NC_000017.10:g.42084796A= , CM000679.1:g.42084796A= GRCh37
NC_000017.9:g.39440322A= NCBI36
NG_008106.1:g.7765A=
NG_023338.1:g.2042T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.1202A= (NAGS) MANE Select ENSP00000293404.2:p.Lys401=
ENST00000293404.7:c.1202A= (NAGS) ENSP00000293404.2:p.Lys401=
ENST00000589767.1:c.1109A= (NAGS) ENSP00000465408.1:p.Lys370=
ENST00000592915.1:n.1090A= (NAGS)
NM_153006.2:c.1202A= (NAGS) NP_694551.1:p.Lys401=
XM_011524438.1:c.1202A= (NAGS) XP_011522740.1:p.Lys401=
XM_011524439.1:c.704A= (NAGS) XP_011522741.1:p.Lys235=
XM_011525035.1:c.-463+16144T= (PYY) XP_011523337.1:n.-463+16144T=
XM_011524439.2:c.704A= (NAGS) XP_011522741.1:p.Lys235=
NM_153006.3:c.1202A= (NAGS) MANE Select NP_694551.1:p.Lys401=