Canonical Allele Identifier: CA555034940

Gene: NAA15

Linked Data

• gnomAD v2: 4-140258158-G-GTTT
• gnomAD v4: 4-139337004-G-GTTT
• MyVariant Identifiers: chr4:g.140258158_140258159insTTT (hg19) ; chr4:g.139337004_139337005insTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139337004_139337005insTTT , CM000666.2:g.139337004_139337005insTTT	GRCh38
NC_000004.11:g.140258158_140258159insTTT , CM000666.1:g.140258158_140258159insTTT	GRCh37
NC_000004.10:g.140477608_140477609insTTT	NCBI36
NG_053037.1:g.40538_40539insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.244+52_244+53insTTT	ENSP00000514912.1:n.244+52_244+53insTTT
ENST00000700275.1:c.244+52_244+53insTTT	ENSP00000514910.1:n.244+52_244+53insTTT
ENST00000700276.1:c.139+2746_139+2747insTTT	ENSP00000514911.1:n.139+2746_139+2747insTTT
ENST00000700277.1:c.240+56_240+57insTTT	ENSP00000514913.1:n.240+56_240+57insTTT
ENST00000700278.1:n.421+52_421+53insTTT
ENST00000700279.1:n.502+52_502+53insTTT
ENST00000296543.10:c.244+52_244+53insTTT MANE Select	ENSP00000296543.4:n.244+52_244+53insTTT
ENST00000296543.9:c.244+52_244+53insTTT	ENSP00000296543.4:n.244+52_244+53insTTT
ENST00000398947.1:c.244+52_244+53insTTT	ENSP00000381920.1:n.244+52_244+53insTTT
ENST00000480277.2:n.80+52_80+53insTTT
ENST00000482087.1:n.388+52_388+53insTTT
NM_057175.3:c.244+52_244+53insTTT	NP_476516.1:n.244+52_244+53insTTT
XM_005263236.1:c.244+52_244+53insTTT	XP_005263293.1:n.244+52_244+53insTTT
NM_057175.4:c.244+52_244+53insTTT	NP_476516.1:n.244+52_244+53insTTT
XM_005263236.3:c.244+52_244+53insTTT	XP_005263293.1:n.244+52_244+53insTTT
NM_057175.5:c.244+52_244+53insTTT MANE Select	NP_476516.1:n.244+52_244+53insTTT