Canonical Allele Identifier: CA3083335

Gene: NAA15

Linked Data

• dbSNP Id: rs754079990
• ExAC: 4:140257978 TTTC / T
• gnomAD v2: 4-140257978-TTTC-T
• gnomAD v3: 4-139336824-TTTC-T
• gnomAD v4: 4-139336824-TTTC-T
• MyVariant Identifiers: chr4:g.140257979_140257981del (hg19) ; chr4:g.139336825_139336827del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336830_139336832del , CM000666.2:g.139336830_139336832del	GRCh38
NC_000004.11:g.140257984_140257986del , CM000666.1:g.140257984_140257986del	GRCh37
NC_000004.10:g.140477434_140477436del	NCBI36
NG_053037.1:g.40364_40366del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.140-18_140-16del	ENSP00000514912.1:n.140-18_140-16del
ENST00000700275.1:c.140-18_140-16del	ENSP00000514910.1:n.140-18_140-16del
ENST00000700276.1:c.139+2572_139+2574del	ENSP00000514911.1:n.139+2572_139+2574del
ENST00000700277.1:c.140-18_140-16del	ENSP00000514913.1:n.140-18_140-16del
ENST00000700278.1:n.317-18_317-16del
ENST00000700279.1:n.398-18_398-16del
ENST00000296543.10:c.140-18_140-16del MANE Select	ENSP00000296543.4:n.140-18_140-16del
ENST00000296543.9:c.140-18_140-16del	ENSP00000296543.4:n.140-18_140-16del
ENST00000398947.1:c.140-18_140-16del	ENSP00000381920.1:n.140-18_140-16del
ENST00000482087.1:n.284-18_284-16del
NM_057175.3:c.140-18_140-16del	NP_476516.1:n.140-18_140-16del
XM_005263236.1:c.140-18_140-16del	XP_005263293.1:n.140-18_140-16del
NM_057175.4:c.140-18_140-16del	NP_476516.1:n.140-18_140-16del
XM_005263236.3:c.140-18_140-16del	XP_005263293.1:n.140-18_140-16del
NM_057175.5:c.140-18_140-16del MANE Select	NP_476516.1:n.140-18_140-16del