Canonical Allele Identifier: CA2514871702

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44005980C>A , CM000679.2:g.44005980C>A GRCh38
NC_000017.10:g.42083348C>A , CM000679.1:g.42083348C>A GRCh37
NC_000017.9:g.39438874C>A NCBI36
NG_008106.1:g.6317C>A
NG_023338.1:g.3490G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.702-44C>A (NAGS) MANE Select ENSP00000293404.2:n.702-44C>A
ENST00000293404.7:c.702-44C>A (NAGS) ENSP00000293404.2:n.702-44C>A
ENST00000589767.1:c.609-44C>A (NAGS) ENSP00000465408.1:n.609-44C>A
NM_153006.2:c.702-44C>A (NAGS) NP_694551.1:n.702-44C>A
XM_011524438.1:c.702-44C>A (NAGS) XP_011522740.1:n.702-44C>A
XM_011524439.1:c.204-44C>A (NAGS) XP_011522741.1:n.204-44C>A
XM_011525035.1:c.-463+17592G>T (PYY) XP_011523337.1:n.-463+17592G>T
XM_011524439.2:c.204-44C>A (NAGS) XP_011522741.1:n.204-44C>A
NM_153006.3:c.702-44C>A (NAGS) MANE Select NP_694551.1:n.702-44C>A