Canonical Allele Identifier: CA394662810
Gene: NAGPA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.5028956C>A , CM000678.2:g.5028956C>A GRCh38
NC_000016.9:g.5078957C>A , CM000678.1:g.5078957C>A GRCh37
NC_000016.8:g.5018958C>A NCBI36
NG_028152.1:g.9986G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000312251.8:c.844G>T MANE Select ENSP00000310998.3:p.Ala282Ser
ENST00000649828.1:c.844G>T ENSP00000498032.1:p.Ala282Ser
ENST00000312251.7:c.844G>T ENSP00000310998.3:p.Ala282Ser
ENST00000381955.7:c.844G>T ENSP00000371381.3:p.Ala282Ser
ENST00000562037.1:c.605G>T ENSP00000464994.1:n.605G>T
ENST00000562346.2:c.505-771G>T
ENST00000562746.5:c.844G>T ENSP00000455900.1:p.Ala282Ser
ENST00000563578.5:c.662G>T
ENST00000564397.5:n.1203G>T
ENST00000565876.5:c.480+1429G>T
ENST00000567739.5:n.163G>T
ENST00000568202.5:n.707G>T
ENST00000569296.5:c.388G>T ENSP00000465949.1:p.Ala130Ser
NM_016256.3:c.844G>T NP_057340.2:p.Ala282Ser
XM_011522517.1:c.844G>T XP_011520819.1:p.Ala282Ser
XM_011522518.1:c.844G>T XP_011520820.1:p.Ala282Ser
XM_011522519.1:c.844G>T XP_011520821.1:p.Ala282Ser
XR_243285.1:n.871G>T
XM_011522517.3:c.844G>T XP_011520819.1:p.Ala282Ser
XR_001751908.2:n.870G>T
XR_001751909.2:n.870G>T
XR_001751910.2:n.870G>T
XR_001751911.2:n.870G>T
XR_001751912.2:n.870G>T
NM_016256.4:c.844G>T MANE Select NP_057340.2:p.Ala282Ser