Canonical Allele Identifier: CA2261181900

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44005991G= , CM000679.2:g.44005991G= GRCh38
NC_000017.10:g.42083359G= , CM000679.1:g.42083359G= GRCh37
NC_000017.9:g.39438885G= NCBI36
NG_008106.1:g.6328G=
NG_023338.1:g.3479C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000293404.8:c.702-33G= (NAGS) MANE Select ENSP00000293404.2:n.702-33G=
ENST00000293404.7:c.702-33G= (NAGS) ENSP00000293404.2:n.702-33G=
ENST00000589767.1:c.609-33G= (NAGS) ENSP00000465408.1:n.609-33G=
NM_153006.2:c.702-33G= (NAGS) NP_694551.1:n.702-33G=
XM_011524438.1:c.702-33G= (NAGS) XP_011522740.1:n.702-33G=
XM_011524439.1:c.204-33G= (NAGS) XP_011522741.1:n.204-33G=
XM_011525035.1:c.-463+17581C= (PYY) XP_011523337.1:n.-463+17581C=
XM_011524439.2:c.204-33G= (NAGS) XP_011522741.1:n.204-33G=
NM_153006.3:c.702-33G= (NAGS) MANE Select NP_694551.1:n.702-33G=