Canonical Allele Identifier: CA2490796182

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218805C= , CM000664.2:g.15218805C=	GRCh38
NC_000002.11:g.15358929C= , CM000664.1:g.15358929C=	GRCh37
NC_000002.10:g.15276380C=	NCBI36
NG_032964.1:g.347544G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700061.1:c.4386G=
ENST00000700062.1:c.4426+13617G=
ENST00000700063.1:c.911G=
ENST00000700064.1:c.2256G=
ENST00000281513.10:c.6400G= MANE Select	ENSP00000281513.5:p.Ala2134=
ENST00000281513.9:c.6400G=	ENSP00000281513.5:p.Ala2134=
ENST00000417461.5:c.512+13617G=	ENSP00000392421.1:n.512+13617G=
ENST00000442506.5:c.3543G=
NM_015909.3:c.6400G=	NP_056993.2:p.Ala2134=
NR_052013.2:n.6280+13617G=
XM_011510357.1:c.6271G=	XP_011508659.1:p.Ala2091=
XM_011510358.1:c.6400G=	XP_011508660.1:p.Ala2134=
XM_011510359.1:c.5761G=	XP_011508661.1:p.Ala1921=
XM_011510360.1:c.4201G=	XP_011508662.1:p.Ala1401=
XM_011510361.1:c.4192G=	XP_011508663.1:p.Ala1398=
XM_011510357.2:c.6271G=	XP_011508659.1:p.Ala2091=
XM_011510358.2:c.6400G=	XP_011508660.1:p.Ala2134=
XM_011510360.2:c.4201G=	XP_011508662.1:p.Ala1401=
XM_011510361.2:c.4192G=	XP_011508663.1:p.Ala1398=
XM_017004317.1:c.6400G=	XP_016859806.1:p.Ala2134=
XM_024452961.1:c.5761G=	XP_024308729.1:p.Ala1921=
NM_015909.4:c.6400G= MANE Select	NP_056993.2:p.Ala2134=
NR_052013.3:n.6266+13617G=