Canonical Allele Identifier: CA1498317947

Gene: NAA15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336946_139336948delinsCAT , CM000666.2:g.139336946_139336948delinsCAT	GRCh38
NC_000004.11:g.140258100_140258102delinsCAT , CM000666.1:g.140258100_140258102delinsCAT	GRCh37
NC_000004.10:g.140477550_140477552delinsCAT	NCBI36
NG_053037.1:g.40480_40482delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.238_240delinsCAT	ENSP00000514912.1:p.His80=
ENST00000700275.1:c.238_240delinsCAT	ENSP00000514910.1:p.His80=
ENST00000700276.1:c.139+2688_139+2690delinsCAT	ENSP00000514911.1:n.139+2688_139+2690delinsCAT
ENST00000700277.1:c.238_240delinsCAT	ENSP00000514913.1:p.His80=
ENST00000700278.1:n.415_417delinsCAT
ENST00000700279.1:n.496_498delinsCAT
ENST00000296543.10:c.238_240delinsCAT MANE Select	ENSP00000296543.4:p.His80=
ENST00000296543.9:c.238_240delinsCAT	ENSP00000296543.4:p.His80=
ENST00000398947.1:c.238_240delinsCAT	ENSP00000381920.1:p.His80=
ENST00000480277.2:n.74_76delinsCAT
ENST00000482087.1:n.382_384delinsCAT
NM_057175.3:c.238_240delinsCAT	NP_476516.1:p.His80=
XM_005263236.1:c.238_240delinsCAT	XP_005263293.1:p.His80=
NM_057175.4:c.238_240delinsCAT	NP_476516.1:p.His80=
XM_005263236.3:c.238_240delinsCAT	XP_005263293.1:p.His80=
NM_057175.5:c.238_240delinsCAT MANE Select	NP_476516.1:p.His80=