Canonical Allele Identifier: CA2805664231
Gene: NAGPA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.5027964_5027965insCCCACCCCCCCCCCCCCCCCCTCCCC , CM000678.2:g.5027964_5027965insCCCACCCCCCCCCCCCCCCCCTCCCC GRCh38
NC_000016.9:g.5077965_5077966insCCCACCCCCCCCCCCCCCCCCTCCCC , CM000678.1:g.5077965_5077966insCCCACCCCCCCCCCCCCCCCCTCCCC GRCh37
NC_000016.8:g.5017966_5017967insCCCACCCCCCCCCCCCCCCCCTCCCC NCBI36
NG_028152.1:g.10987_10988insGGGGGGGGGGGGTGGGGGGGAGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000312251.8:c.1126+25_1126+26insGGGGGGGGGGGGTGGGGGGGAGGGGG MANE Select ENSP00000310998.3:n.1126+25_1126+26insGGGGGGGGGGGGTGGGGGGGAGG...
ENST00000649828.1:c.*298+25_*298+26insGGGGGGGGGGGGTGGGGGGGAGGGGG ENSP00000498032.1:n.*298+25_*298+26insGGGGGGGGGGGGTGGGGGGGAGG...
ENST00000312251.7:c.1126+25_1126+26insGGGGGGGGGGGGTGGGGGGGAGGGGG ENSP00000310998.3:n.1126+25_1126+26insGGGGGGGGGGGGTGGGGGGGAGG...
ENST00000381955.7:c.1126+25_1126+26insGGGGGGGGGGGGTGGGGGGGAGGGGG ENSP00000371381.3:n.1126+25_1126+26insGGGGGGGGGGGGTGGGGGGGAGG...
ENST00000562746.5:c.*298+25_*298+26insGGGGGGGGGGGGTGGGGGGGAGGGGG ENSP00000455900.1:n.*298+25_*298+26insGGGGGGGGGGGGTGGGGGGGAGG...
ENST00000563578.5:c.738+925_738+926insGGGGGGGGGGGGTGGGGGGGAGGGGG
ENST00000564397.5:n.2179+25_2179+26insGGGGGGGGGGGGTGGGGGGGAGGGGG
ENST00000565876.5:c.481-576_481-575insGGGGGGGGGGGGTGGGGGGGAGGGGG
ENST00000566137.5:n.424+25_424+26insGGGGGGGGGGGGTGGGGGGGAGGGGG
ENST00000567739.5:n.445+25_445+26insGGGGGGGGGGGGTGGGGGGGAGGGGG
ENST00000568202.5:n.989+25_989+26insGGGGGGGGGGGGTGGGGGGGAGGGGG
ENST00000569296.5:c.739+25_739+26insGGGGGGGGGGGGTGGGGGGGAGGGGG ENSP00000465949.1:n.739+25_739+26insGGGGGGGGGGGGTGGGGGGGAGGGG...
NM_016256.3:c.1126+25_1126+26insGGGGGGGGGGGGTGGGGGGGAGGGGG NP_057340.2:n.1126+25_1126+26insGGGGGGGGGGGGTGGGGGGGAGGGGG
XM_011522517.1:c.1126+25_1126+26insGGGGGGGGGGGGTGGGGGGGAGGGGG XP_011520819.1:n.1126+25_1126+26insGGGGGGGGGGGGTGGGGGGGAGGGGG...
XR_243285.1:n.1222+25_1222+26insGGGGGGGGGGGGTGGGGGGGAGGGGG
XM_011522517.3:c.1126+25_1126+26insGGGGGGGGGGGGTGGGGGGGAGGGGG XP_011520819.1:n.1126+25_1126+26insGGGGGGGGGGGGTGGGGGGGAGGGGG...
XR_001751908.2:n.1221+25_1221+26insGGGGGGGGGGGGTGGGGGGGAGGGGG
XR_001751909.2:n.1225+25_1225+26insGGGGGGGGGGGGTGGGGGGGAGGGGG
XR_001751910.2:n.1254+25_1254+26insGGGGGGGGGGGGTGGGGGGGAGGGGG
XR_001751911.2:n.1254+25_1254+26insGGGGGGGGGGGGTGGGGGGGAGGGGG
XR_001751912.2:n.1258+25_1258+26insGGGGGGGGGGGGTGGGGGGGAGGGGG
NM_016256.4:c.1126+25_1126+26insGGGGGGGGGGGGTGGGGGGGAGGGGG MANE Select NP_057340.2:n.1126+25_1126+26insGGGGGGGGGGGGTGGGGGGGAGGGGG