Canonical Allele Identifier: CA2672126004
Gene: NAA15 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.139336932del , CM000666.2:g.139336932del GRCh38
NC_000004.11:g.140258086del , CM000666.1:g.140258086del GRCh37
NC_000004.10:g.140477536del NCBI36
NG_053037.1:g.40466del

Transcript Alleles

HGVS Amino-acid Change
ENST00000468029.2:c.224del ENSP00000514912.1:p.Asn75MetfsTer3
ENST00000700275.1:c.224del ENSP00000514910.1:p.Asn75MetfsTer3
ENST00000700276.1:c.139+2674del ENSP00000514911.1:n.139+2674del
ENST00000700277.1:c.224del ENSP00000514913.1:p.Asn75MetfsTer3
ENST00000700278.1:n.401del
ENST00000700279.1:n.482del
ENST00000296543.10:c.224del MANE Select ENSP00000296543.4:p.Asn75MetfsTer3
ENST00000296543.9:c.224del ENSP00000296543.4:p.Asn75MetfsTer3
ENST00000398947.1:c.224del ENSP00000381920.1:p.Asn75MetfsTer3
ENST00000480277.2:n.60del
ENST00000482087.1:n.368del
NM_057175.3:c.224del NP_476516.1:p.Asn75MetfsTer3
XM_005263236.1:c.224del XP_005263293.1:p.Asn75MetfsTer3
NM_057175.4:c.224del NP_476516.1:p.Asn75MetfsTer3
XM_005263236.3:c.224del XP_005263293.1:p.Asn75MetfsTer3
NM_057175.5:c.224del MANE Select NP_476516.1:p.Asn75MetfsTer3