Canonical Allele Identifier: CA394662853
Gene: NAGPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.5028966G>C , CM000678.2:g.5028966G>C GRCh38
NC_000016.9:g.5078967G>C , CM000678.1:g.5078967G>C GRCh37
NC_000016.8:g.5018968G>C NCBI36
NG_028152.1:g.9976C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000312251.8:c.834C>G MANE Select ENSP00000310998.3:p.Asp278Glu
ENST00000649828.1:c.834C>G ENSP00000498032.1:p.Asp278Glu
ENST00000312251.7:c.834C>G ENSP00000310998.3:p.Asp278Glu
ENST00000381955.7:c.834C>G ENSP00000371381.3:p.Asp278Glu
ENST00000562037.1:c.595C>G ENSP00000464994.1:n.595C>G
ENST00000562346.2:c.505-781C>G
ENST00000562746.5:c.834C>G ENSP00000455900.1:p.Asp278Glu
ENST00000563578.5:c.652C>G
ENST00000564397.5:n.1193C>G
ENST00000565876.5:c.480+1419C>G
ENST00000567739.5:n.153C>G
ENST00000568202.5:n.697C>G
ENST00000569296.5:c.378C>G ENSP00000465949.1:p.Asp126Glu
NM_016256.3:c.834C>G NP_057340.2:p.Asp278Glu
XM_011522517.1:c.834C>G XP_011520819.1:p.Asp278Glu
XM_011522518.1:c.834C>G XP_011520820.1:p.Asp278Glu
XM_011522519.1:c.834C>G XP_011520821.1:p.Asp278Glu
XR_243285.1:n.861C>G
XM_011522517.3:c.834C>G XP_011520819.1:p.Asp278Glu
XR_001751908.2:n.860C>G
XR_001751909.2:n.860C>G
XR_001751910.2:n.860C>G
XR_001751911.2:n.860C>G
XR_001751912.2:n.860C>G
NM_016256.4:c.834C>G MANE Select NP_057340.2:p.Asp278Glu