Canonical Allele Identifier: CA1498317793

Gene: NAA15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336804_139336805delinsTA , CM000666.2:g.139336804_139336805delinsTA	GRCh38
NC_000004.11:g.140257958_140257959delinsTA , CM000666.1:g.140257958_140257959delinsTA	GRCh37
NC_000004.10:g.140477408_140477409delinsTA	NCBI36
NG_053037.1:g.40338_40339delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.140-44_140-43delinsTA	ENSP00000514912.1:n.140-44_140-43delinsTA
ENST00000700275.1:c.140-44_140-43delinsTA	ENSP00000514910.1:n.140-44_140-43delinsTA
ENST00000700276.1:c.139+2546_139+2547delinsTA	ENSP00000514911.1:n.139+2546_139+2547delinsTA
ENST00000700277.1:c.140-44_140-43delinsTA	ENSP00000514913.1:n.140-44_140-43delinsTA
ENST00000700278.1:n.317-44_317-43delinsTA
ENST00000700279.1:n.398-44_398-43delinsTA
ENST00000296543.10:c.140-44_140-43delinsTA MANE Select	ENSP00000296543.4:n.140-44_140-43delinsTA
ENST00000296543.9:c.140-44_140-43delinsTA	ENSP00000296543.4:n.140-44_140-43delinsTA
ENST00000398947.1:c.140-44_140-43delinsTA	ENSP00000381920.1:n.140-44_140-43delinsTA
ENST00000482087.1:n.284-44_284-43delinsTA
NM_057175.3:c.140-44_140-43delinsTA	NP_476516.1:n.140-44_140-43delinsTA
XM_005263236.1:c.140-44_140-43delinsTA	XP_005263293.1:n.140-44_140-43delinsTA
NM_057175.4:c.140-44_140-43delinsTA	NP_476516.1:n.140-44_140-43delinsTA
XM_005263236.3:c.140-44_140-43delinsTA	XP_005263293.1:n.140-44_140-43delinsTA
NM_057175.5:c.140-44_140-43delinsTA MANE Select	NP_476516.1:n.140-44_140-43delinsTA