Canonical Allele Identifier: CA2203673392
Gene: NAGPA HGNC NCBI

Linked Data

dbSNP Id: rs1956025136

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.5027587A>T , CM000678.2:g.5027587A>T GRCh38
NC_000016.9:g.5077588A>T , CM000678.1:g.5077588A>T GRCh37
NC_000016.8:g.5017589A>T NCBI36
NG_028152.1:g.11355T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000312251.8:c.1175-208T>A MANE Select ENSP00000310998.3:n.1175-208T>A
ENST00000649828.1:c.*347-208T>A ENSP00000498032.1:n.*347-208T>A
ENST00000312251.7:c.1175-208T>A ENSP00000310998.3:n.1175-208T>A
ENST00000381955.7:c.1174+259T>A ENSP00000371381.3:n.1174+259T>A
ENST00000562746.5:c.*347-208T>A ENSP00000455900.1:n.*347-208T>A
ENST00000563578.5:c.738+1293T>A
ENST00000564397.5:n.2228-208T>A
ENST00000565876.5:c.481-208T>A
ENST00000566137.5:n.473-208T>A
ENST00000567739.5:n.494-208T>A
ENST00000568202.5:n.1038-208T>A
ENST00000569296.5:c.788-208T>A ENSP00000465949.1:n.788-208T>A
NM_016256.3:c.1175-208T>A NP_057340.2:n.1175-208T>A
XM_011522517.1:c.1175-208T>A XP_011520819.1:n.1175-208T>A
XR_243285.1:n.1271-208T>A
XM_011522517.3:c.1175-208T>A XP_011520819.1:n.1175-208T>A
XR_001751908.2:n.1270-208T>A
XR_001751909.2:n.1274-208T>A
XR_001751910.2:n.1303-208T>A
XR_001751911.2:n.1303-208T>A
XR_001751912.2:n.1307-208T>A
NM_016256.4:c.1175-208T>A MANE Select NP_057340.2:n.1175-208T>A