Canonical Allele Identifier: CA2672126025

Gene: NAA15

Linked Data

• gnomAD v4: 4-139336977-G-GGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336978_139336979insCTG , CM000666.2:g.139336978_139336979insCTG	GRCh38
NC_000004.11:g.140258132_140258133insCTG , CM000666.1:g.140258132_140258133insCTG	GRCh37
NC_000004.10:g.140477582_140477583insCTG	NCBI36
NG_053037.1:g.40512_40513insCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.244+26_244+27insCTG	ENSP00000514912.1:n.244+26_244+27insCTG
ENST00000700275.1:c.244+26_244+27insCTG	ENSP00000514910.1:n.244+26_244+27insCTG
ENST00000700276.1:c.139+2720_139+2721insCTG	ENSP00000514911.1:n.139+2720_139+2721insCTG
ENST00000700277.1:c.240+30_240+31insCTG	ENSP00000514913.1:n.240+30_240+31insCTG
ENST00000700278.1:n.421+26_421+27insCTG
ENST00000700279.1:n.502+26_502+27insCTG
ENST00000296543.10:c.244+26_244+27insCTG MANE Select	ENSP00000296543.4:n.244+26_244+27insCTG
ENST00000296543.9:c.244+26_244+27insCTG	ENSP00000296543.4:n.244+26_244+27insCTG
ENST00000398947.1:c.244+26_244+27insCTG	ENSP00000381920.1:n.244+26_244+27insCTG
ENST00000480277.2:n.80+26_80+27insCTG
ENST00000482087.1:n.388+26_388+27insCTG
NM_057175.3:c.244+26_244+27insCTG	NP_476516.1:n.244+26_244+27insCTG
XM_005263236.1:c.244+26_244+27insCTG	XP_005263293.1:n.244+26_244+27insCTG
NM_057175.4:c.244+26_244+27insCTG	NP_476516.1:n.244+26_244+27insCTG
XM_005263236.3:c.244+26_244+27insCTG	XP_005263293.1:n.244+26_244+27insCTG
NM_057175.5:c.244+26_244+27insCTG MANE Select	NP_476516.1:n.244+26_244+27insCTG