Canonical Allele Identifier: CA1498317758

Gene: NAA15

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.139336759T= , CM000666.2:g.139336759T=	GRCh38
NC_000004.11:g.140257913T= , CM000666.1:g.140257913T=	GRCh37
NC_000004.10:g.140477363T=	NCBI36
NG_053037.1:g.40293T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468029.2:c.140-89T=	ENSP00000514912.1:n.140-89T=
ENST00000700275.1:c.140-89T=	ENSP00000514910.1:n.140-89T=
ENST00000700276.1:c.139+2501T=	ENSP00000514911.1:n.139+2501T=
ENST00000700277.1:c.140-89T=	ENSP00000514913.1:n.140-89T=
ENST00000700278.1:n.317-89T=
ENST00000700279.1:n.398-89T=
ENST00000296543.10:c.140-89T= MANE Select	ENSP00000296543.4:n.140-89T=
ENST00000296543.9:c.140-89T=	ENSP00000296543.4:n.140-89T=
ENST00000398947.1:c.140-89T=	ENSP00000381920.1:n.140-89T=
ENST00000482087.1:n.284-89T=
NM_057175.3:c.140-89T=	NP_476516.1:n.140-89T=
XM_005263236.1:c.140-89T=	XP_005263293.1:n.140-89T=
NM_057175.4:c.140-89T=	NP_476516.1:n.140-89T=
XM_005263236.3:c.140-89T=	XP_005263293.1:n.140-89T=
NM_057175.5:c.140-89T= MANE Select	NP_476516.1:n.140-89T=