Canonical Allele Identifier: CA1068687426

Gene: NAA15

Linked Data

• dbSNP Id: rs1747215940
• gnomAD v3: 4-139336818-GTTCCTT-G
• gnomAD v4: 4-139336818-GTTCCTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336822_139336827del , CM000666.2:g.139336822_139336827del	GRCh38
NC_000004.11:g.140257976_140257981del , CM000666.1:g.140257976_140257981del	GRCh37
NC_000004.10:g.140477426_140477431del	NCBI36
NG_053037.1:g.40356_40361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.140-26_140-21del	ENSP00000514912.1:n.140-26_140-21del
ENST00000700275.1:c.140-26_140-21del	ENSP00000514910.1:n.140-26_140-21del
ENST00000700276.1:c.139+2564_139+2569del	ENSP00000514911.1:n.139+2564_139+2569del
ENST00000700277.1:c.140-26_140-21del	ENSP00000514913.1:n.140-26_140-21del
ENST00000700278.1:n.317-26_317-21del
ENST00000700279.1:n.398-26_398-21del
ENST00000296543.10:c.140-26_140-21del MANE Select	ENSP00000296543.4:n.140-26_140-21del
ENST00000296543.9:c.140-26_140-21del	ENSP00000296543.4:n.140-26_140-21del
ENST00000398947.1:c.140-26_140-21del	ENSP00000381920.1:n.140-26_140-21del
ENST00000482087.1:n.284-26_284-21del
NM_057175.3:c.140-26_140-21del	NP_476516.1:n.140-26_140-21del
XM_005263236.1:c.140-26_140-21del	XP_005263293.1:n.140-26_140-21del
NM_057175.4:c.140-26_140-21del	NP_476516.1:n.140-26_140-21del
XM_005263236.3:c.140-26_140-21del	XP_005263293.1:n.140-26_140-21del
NM_057175.5:c.140-26_140-21del MANE Select	NP_476516.1:n.140-26_140-21del