Canonical Allele Identifier: CA2203660362
Gene: NAGPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.5029050_5029051delinsTC , CM000678.2:g.5029050_5029051delinsTC GRCh38
NC_000016.9:g.5079051_5079052delinsTC , CM000678.1:g.5079051_5079052delinsTC GRCh37
NC_000016.8:g.5019052_5019053delinsTC NCBI36
NG_028152.1:g.9891_9892delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000312251.8:c.792-43_792-42delinsGA MANE Select ENSP00000310998.3:n.792-43_792-42delinsGA
ENST00000649828.1:c.792-43_792-42delinsGA ENSP00000498032.1:n.792-43_792-42delinsGA
ENST00000312251.7:c.792-43_792-42delinsGA ENSP00000310998.3:n.792-43_792-42delinsGA
ENST00000381955.7:c.792-43_792-42delinsGA ENSP00000371381.3:n.792-43_792-42delinsGA
ENST00000562037.1:c.553-43_553-42delinsGA ENSP00000464994.1:n.553-43_553-42delinsGA
ENST00000562346.2:c.505-866_505-865delinsGA
ENST00000562746.5:c.792-43_792-42delinsGA ENSP00000455900.1:n.792-43_792-42delinsGA
ENST00000563578.5:c.610-43_610-42delinsGA
ENST00000564397.5:n.1108_1109delinsGA
ENST00000565876.5:c.480+1334_480+1335delinsGA
ENST00000567739.5:n.68_69delinsGA
ENST00000568202.5:n.655-43_655-42delinsGA
ENST00000569296.5:c.336-43_336-42delinsGA ENSP00000465949.1:n.336-43_336-42delinsGA
NM_016256.3:c.792-43_792-42delinsGA NP_057340.2:n.792-43_792-42delinsGA
XM_011522517.1:c.792-43_792-42delinsGA XP_011520819.1:n.792-43_792-42delinsGA
XM_011522518.1:c.792-43_792-42delinsGA XP_011520820.1:n.792-43_792-42delinsGA
XM_011522519.1:c.792-43_792-42delinsGA XP_011520821.1:n.792-43_792-42delinsGA
XR_243285.1:n.819-43_819-42delinsGA
XM_011522517.3:c.792-43_792-42delinsGA XP_011520819.1:n.792-43_792-42delinsGA
XR_001751908.2:n.818-43_818-42delinsGA
XR_001751909.2:n.818-43_818-42delinsGA
XR_001751910.2:n.818-43_818-42delinsGA
XR_001751911.2:n.818-43_818-42delinsGA
XR_001751912.2:n.818-43_818-42delinsGA
NM_016256.4:c.792-43_792-42delinsGA MANE Select NP_057340.2:n.792-43_792-42delinsGA