Canonical Allele Identifier: CA2580071548

Gene: NAA15

Linked Data

• ClinVar Variation Id: 2032790
• ClinVar RCV Id: RCV002881436

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336839_139336845del , CM000666.2:g.139336839_139336845del	GRCh38
NC_000004.11:g.140257993_140257999del , CM000666.1:g.140257993_140257999del	GRCh37
NC_000004.10:g.140477443_140477449del	NCBI36
NG_053037.1:g.40373_40379del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.140-9_140-3del	ENSP00000514912.1:n.140-9_140-3del
ENST00000700275.1:c.140-9_140-3del	ENSP00000514910.1:n.140-9_140-3del
ENST00000700276.1:c.139+2581_139+2587del	ENSP00000514911.1:n.139+2581_139+2587del
ENST00000700277.1:c.140-9_140-3del	ENSP00000514913.1:n.140-9_140-3del
ENST00000700278.1:n.317-9_317-3del
ENST00000700279.1:n.398-9_398-3del
ENST00000296543.10:c.140-9_140-3del MANE Select	ENSP00000296543.4:n.140-9_140-3del
ENST00000296543.9:c.140-9_140-3del	ENSP00000296543.4:n.140-9_140-3del
ENST00000398947.1:c.140-9_140-3del	ENSP00000381920.1:n.140-9_140-3del
ENST00000482087.1:n.284-9_284-3del
NM_057175.3:c.140-9_140-3del	NP_476516.1:n.140-9_140-3del
XM_005263236.1:c.140-9_140-3del	XP_005263293.1:n.140-9_140-3del
NM_057175.4:c.140-9_140-3del	NP_476516.1:n.140-9_140-3del
XM_005263236.3:c.140-9_140-3del	XP_005263293.1:n.140-9_140-3del
NM_057175.5:c.140-9_140-3del MANE Select	NP_476516.1:n.140-9_140-3del