Canonical Allele Identifier: CA500616124

Linked Data

MyVariant Identifiers: chr17:g.42083527G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44006159G>C , CM000679.2:g.44006159G>C GRCh38
NC_000017.10:g.42083527G>C , CM000679.1:g.42083527G>C GRCh37
NC_000017.9:g.39439053G>C NCBI36
NG_008106.1:g.6496G>C
NG_023338.1:g.3311C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.837G>C (NAGS) MANE Select ENSP00000293404.2:p.Ala279=
ENST00000293404.7:c.837G>C (NAGS) ENSP00000293404.2:p.Ala279=
ENST00000589767.1:c.744G>C (NAGS) ENSP00000465408.1:p.Ala248=
ENST00000592915.1:n.112G>C (NAGS)
NM_153006.2:c.837G>C (NAGS) NP_694551.1:p.Ala279=
XM_011524438.1:c.837G>C (NAGS) XP_011522740.1:p.Ala279=
XM_011524439.1:c.339G>C (NAGS) XP_011522741.1:p.Ala113=
XM_011525035.1:c.-463+17413C>G (PYY) XP_011523337.1:n.-463+17413C>G
XM_011524439.2:c.339G>C (NAGS) XP_011522741.1:p.Ala113=
NM_153006.3:c.837G>C (NAGS) MANE Select NP_694551.1:p.Ala279=