Canonical Allele Identifier: CA2490796214

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218860T= , CM000664.2:g.15218860T=	GRCh38
NC_000002.11:g.15358984T= , CM000664.1:g.15358984T=	GRCh37
NC_000002.10:g.15276435T=	NCBI36
NG_032964.1:g.347489A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4331A=
ENST00000700062.1:c.4426+13562A=
ENST00000700063.1:c.856A=
ENST00000700064.1:c.2201A=
ENST00000281513.10:c.6345A= MANE Select	ENSP00000281513.5:p.Gln2115=
ENST00000281513.9:c.6345A=	ENSP00000281513.5:p.Gln2115=
ENST00000417461.5:c.512+13562A=	ENSP00000392421.1:n.512+13562A=
ENST00000442506.5:c.3488A=
NM_015909.3:c.6345A=	NP_056993.2:p.Gln2115=
NR_052013.2:n.6280+13562A=
XM_011510357.1:c.6216A=	XP_011508659.1:p.Gln2072=
XM_011510358.1:c.6345A=	XP_011508660.1:p.Gln2115=
XM_011510359.1:c.5706A=	XP_011508661.1:p.Gln1902=
XM_011510360.1:c.4146A=	XP_011508662.1:p.Gln1382=
XM_011510361.1:c.4137A=	XP_011508663.1:p.Gln1379=
XM_011510357.2:c.6216A=	XP_011508659.1:p.Gln2072=
XM_011510358.2:c.6345A=	XP_011508660.1:p.Gln2115=
XM_011510360.2:c.4146A=	XP_011508662.1:p.Gln1382=
XM_011510361.2:c.4137A=	XP_011508663.1:p.Gln1379=
XM_017004317.1:c.6345A=	XP_016859806.1:p.Gln2115=
XM_024452961.1:c.5706A=	XP_024308729.1:p.Gln1902=
NM_015909.4:c.6345A= MANE Select	NP_056993.2:p.Gln2115=
NR_052013.3:n.6266+13562A=