Canonical Allele Identifier: CA1498317945
Gene: NAA15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.139336941A= , CM000666.2:g.139336941A= GRCh38
NC_000004.11:g.140258095A= , CM000666.1:g.140258095A= GRCh37
NC_000004.10:g.140477545A= NCBI36
NG_053037.1:g.40475A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000468029.2:c.233A= ENSP00000514912.1:p.Lys78=
ENST00000700275.1:c.233A= ENSP00000514910.1:p.Lys78=
ENST00000700276.1:c.139+2683A= ENSP00000514911.1:n.139+2683A=
ENST00000700277.1:c.233A= ENSP00000514913.1:p.Lys78=
ENST00000700278.1:n.410A=
ENST00000700279.1:n.491A=
ENST00000296543.10:c.233A= MANE Select ENSP00000296543.4:p.Lys78=
ENST00000296543.9:c.233A= ENSP00000296543.4:p.Lys78=
ENST00000398947.1:c.233A= ENSP00000381920.1:p.Lys78=
ENST00000480277.2:n.69A=
ENST00000482087.1:n.377A=
NM_057175.3:c.233A= NP_476516.1:p.Lys78=
XM_005263236.1:c.233A= XP_005263293.1:p.Lys78=
NM_057175.4:c.233A= NP_476516.1:p.Lys78=
XM_005263236.3:c.233A= XP_005263293.1:p.Lys78=
NM_057175.5:c.233A= MANE Select NP_476516.1:p.Lys78=