Canonical Allele Identifier: CA106701924

Gene: NAA15

Linked Data

• dbSNP Id: rs949698923
• gnomAD v3: 4-139336730-ACAT-A
• gnomAD v4: 4-139336730-ACAT-A
• MyVariant Identifiers: chr4:g.140257885_140257887del (hg19) ; chr4:g.139336731_139336733del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336731_139336733del , CM000666.2:g.139336731_139336733del	GRCh38
NC_000004.11:g.140257885_140257887del , CM000666.1:g.140257885_140257887del	GRCh37
NC_000004.10:g.140477335_140477337del	NCBI36
NG_053037.1:g.40265_40267del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.140-117_140-115del	ENSP00000514912.1:n.140-117_140-115del
ENST00000700275.1:c.140-117_140-115del	ENSP00000514910.1:n.140-117_140-115del
ENST00000700276.1:c.139+2473_139+2475del	ENSP00000514911.1:n.139+2473_139+2475del
ENST00000700277.1:c.140-117_140-115del	ENSP00000514913.1:n.140-117_140-115del
ENST00000700278.1:n.317-117_317-115del
ENST00000700279.1:n.398-117_398-115del
ENST00000296543.10:c.140-117_140-115del MANE Select	ENSP00000296543.4:n.140-117_140-115del
ENST00000296543.9:c.140-117_140-115del	ENSP00000296543.4:n.140-117_140-115del
ENST00000398947.1:c.140-117_140-115del	ENSP00000381920.1:n.140-117_140-115del
ENST00000482087.1:n.284-117_284-115del
NM_057175.3:c.140-117_140-115del	NP_476516.1:n.140-117_140-115del
XM_005263236.1:c.140-117_140-115del	XP_005263293.1:n.140-117_140-115del
NM_057175.4:c.140-117_140-115del	NP_476516.1:n.140-117_140-115del
XM_005263236.3:c.140-117_140-115del	XP_005263293.1:n.140-117_140-115del
NM_057175.5:c.140-117_140-115del MANE Select	NP_476516.1:n.140-117_140-115del