Canonical Allele Identifier: CA2490796355

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15219119C= , CM000664.2:g.15219119C=	GRCh38
NC_000002.11:g.15359243C= , CM000664.1:g.15359243C=	GRCh37
NC_000002.10:g.15276694C=	NCBI36
NG_032964.1:g.347230G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4223-151G=
ENST00000700062.1:c.4426+13303G=
ENST00000700063.1:c.748-151G=
ENST00000700064.1:c.2093-151G=
ENST00000281513.10:c.6237-151G= MANE Select	ENSP00000281513.5:n.6237-151G=
ENST00000281513.9:c.6237-151G=	ENSP00000281513.5:n.6237-151G=
ENST00000417461.5:c.512+13303G=	ENSP00000392421.1:n.512+13303G=
ENST00000442506.5:c.3380-151G=
NM_015909.3:c.6237-151G=	NP_056993.2:n.6237-151G=
NR_052013.2:n.6280+13303G=
XM_011510357.1:c.6108-151G=	XP_011508659.1:n.6108-151G=
XM_011510358.1:c.6237-151G=	XP_011508660.1:n.6237-151G=
XM_011510359.1:c.5598-151G=	XP_011508661.1:n.5598-151G=
XM_011510360.1:c.4038-151G=	XP_011508662.1:n.4038-151G=
XM_011510361.1:c.4029-151G=	XP_011508663.1:n.4029-151G=
XM_011510357.2:c.6108-151G=	XP_011508659.1:n.6108-151G=
XM_011510358.2:c.6237-151G=	XP_011508660.1:n.6237-151G=
XM_011510360.2:c.4038-151G=	XP_011508662.1:n.4038-151G=
XM_011510361.2:c.4029-151G=	XP_011508663.1:n.4029-151G=
XM_017004317.1:c.6237-151G=	XP_016859806.1:n.6237-151G=
XM_024452961.1:c.5598-151G=	XP_024308729.1:n.5598-151G=
NM_015909.4:c.6237-151G= MANE Select	NP_056993.2:n.6237-151G=
NR_052013.3:n.6266+13303G=