Canonical Allele Identifier: CA2203660223
Gene: NAGPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.5028980G= , CM000678.2:g.5028980G= GRCh38
NC_000016.9:g.5078981G= , CM000678.1:g.5078981G= GRCh37
NC_000016.8:g.5018982G= NCBI36
NG_028152.1:g.9962C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000312251.8:c.820C= MANE Select ENSP00000310998.3:p.Leu274=
ENST00000649828.1:c.820C= ENSP00000498032.1:p.Leu274=
ENST00000312251.7:c.820C= ENSP00000310998.3:p.Leu274=
ENST00000381955.7:c.820C= ENSP00000371381.3:p.Leu274=
ENST00000562037.1:c.581C= ENSP00000464994.1:n.581C=
ENST00000562346.2:c.505-795C=
ENST00000562746.5:c.820C= ENSP00000455900.1:p.Leu274=
ENST00000563578.5:c.638C=
ENST00000564397.5:n.1179C=
ENST00000565876.5:c.480+1405C=
ENST00000567739.5:n.139C=
ENST00000568202.5:n.683C=
ENST00000569296.5:c.364C= ENSP00000465949.1:p.Leu122=
NM_016256.3:c.820C= NP_057340.2:p.Leu274=
XM_011522517.1:c.820C= XP_011520819.1:p.Leu274=
XM_011522518.1:c.820C= XP_011520820.1:p.Leu274=
XM_011522519.1:c.820C= XP_011520821.1:p.Leu274=
XR_243285.1:n.847C=
XM_011522517.3:c.820C= XP_011520819.1:p.Leu274=
XR_001751908.2:n.846C=
XR_001751909.2:n.846C=
XR_001751910.2:n.846C=
XR_001751911.2:n.846C=
XR_001751912.2:n.846C=
NM_016256.4:c.820C= MANE Select NP_057340.2:p.Leu274=