Canonical Allele Identifier: CA3083328

Gene: NAA15

Linked Data

• dbSNP Id: rs764622162
• ExAC: 4:140257966 TA / T
• MyVariant Identifiers: chr4:g.140257967del (hg19) ; chr4:g.139336813del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336816del , CM000666.2:g.139336816del	GRCh38
NC_000004.11:g.140257970del , CM000666.1:g.140257970del	GRCh37
NC_000004.10:g.140477420del	NCBI36
NG_053037.1:g.40350del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.140-32del	ENSP00000514912.1:n.140-32del
ENST00000700275.1:c.140-32del	ENSP00000514910.1:n.140-32del
ENST00000700276.1:c.139+2558del	ENSP00000514911.1:n.139+2558del
ENST00000700277.1:c.140-32del	ENSP00000514913.1:n.140-32del
ENST00000700278.1:n.317-32del
ENST00000700279.1:n.398-32del
ENST00000296543.10:c.140-32del MANE Select	ENSP00000296543.4:n.140-32del
ENST00000296543.9:c.140-32del	ENSP00000296543.4:n.140-32del
ENST00000398947.1:c.140-32del	ENSP00000381920.1:n.140-32del
ENST00000482087.1:n.284-32del
NM_057175.3:c.140-32del	NP_476516.1:n.140-32del
XM_005263236.1:c.140-32del	XP_005263293.1:n.140-32del
NM_057175.4:c.140-32del	NP_476516.1:n.140-32del
XM_005263236.3:c.140-32del	XP_005263293.1:n.140-32del
NM_057175.5:c.140-32del MANE Select	NP_476516.1:n.140-32del