Canonical Allele Identifier: CA2490940575

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15535954T= , CM000664.2:g.15535954T=	GRCh38
NC_000002.11:g.15676078T= , CM000664.1:g.15676078T=	GRCh37
NC_000002.10:g.15593529T=	NCBI36
NG_032964.1:g.30395A=

Transcript Alleles

HGVS	Amino-acid Change
NM_015909.4:c.647+464A= MANE Select	NP_056993.2:n.647+464A=
ENST00000281513.10:c.647+464A= MANE Select	ENSP00000281513.5:n.647+464A=
NM_015909.3:c.647+464A=	NP_056993.2:n.647+464A=
NR_052013.2:n.691+464A=
NR_052013.3:n.677+464A=
ENST00000281513.9:c.647+464A=	ENSP00000281513.5:n.647+464A=
ENST00000700065.1:n.660+464A=
ENST00000700066.1:c.164+464A=	ENSP00000514780.1:n.164+464A=
ENST00000700067.1:n.662+464A=
ENST00000700068.1:n.662+464A=
ENST00000700069.1:c.647+464A=	ENSP00000514781.1:n.647+464A=
ENST00000700070.1:c.*306+464A=	ENSP00000514782.1:n.*306+464A=
ENST00000700071.1:n.677+464A=
XM_011510357.1:c.647+464A=	XP_011508659.1:n.647+464A=
XM_011510357.2:c.647+464A=	XP_011508659.1:n.647+464A=
XM_011510358.1:c.647+464A=	XP_011508660.1:n.647+464A=
XM_011510358.2:c.647+464A=	XP_011508660.1:n.647+464A=
XM_011510359.1:c.9-1313A=	XP_011508661.1:n.9-1313A=
XM_017004317.1:c.647+464A=	XP_016859806.1:n.647+464A=
XM_024452961.1:c.9-1313A=	XP_024308729.1:n.9-1313A=