Canonical Allele Identifier: CA1498317673

Gene: NAA15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336652_139336654delinsCTG , CM000666.2:g.139336652_139336654delinsCTG	GRCh38
NC_000004.11:g.140257806_140257808delinsCTG , CM000666.1:g.140257806_140257808delinsCTG	GRCh37
NC_000004.10:g.140477256_140477258delinsCTG	NCBI36
NG_053037.1:g.40186_40188delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.140-196_140-194delinsCTG	ENSP00000514912.1:n.140-196_140-194delinsCTG
ENST00000700275.1:c.140-196_140-194delinsCTG	ENSP00000514910.1:n.140-196_140-194delinsCTG
ENST00000700276.1:c.139+2394_139+2396delinsCTG	ENSP00000514911.1:n.139+2394_139+2396delinsCTG
ENST00000700277.1:c.140-196_140-194delinsCTG	ENSP00000514913.1:n.140-196_140-194delinsCTG
ENST00000700278.1:n.317-196_317-194delinsCTG
ENST00000700279.1:n.398-196_398-194delinsCTG
ENST00000296543.10:c.140-196_140-194delinsCTG MANE Select	ENSP00000296543.4:n.140-196_140-194delinsCTG
ENST00000296543.9:c.140-196_140-194delinsCTG	ENSP00000296543.4:n.140-196_140-194delinsCTG
ENST00000398947.1:c.140-196_140-194delinsCTG	ENSP00000381920.1:n.140-196_140-194delinsCTG
ENST00000482087.1:n.284-196_284-194delinsCTG
NM_057175.3:c.140-196_140-194delinsCTG	NP_476516.1:n.140-196_140-194delinsCTG
XM_005263236.1:c.140-196_140-194delinsCTG	XP_005263293.1:n.140-196_140-194delinsCTG
NM_057175.4:c.140-196_140-194delinsCTG	NP_476516.1:n.140-196_140-194delinsCTG
XM_005263236.3:c.140-196_140-194delinsCTG	XP_005263293.1:n.140-196_140-194delinsCTG
NM_057175.5:c.140-196_140-194delinsCTG MANE Select	NP_476516.1:n.140-196_140-194delinsCTG