Canonical Allele Identifier: CA2490889327

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424385T= , CM000664.2:g.15424385T=	GRCh38
NC_000002.11:g.15564509T= , CM000664.1:g.15564509T=	GRCh37
NC_000002.10:g.15481960T=	NCBI36
NG_032964.1:g.141964A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.604A=
ENST00000700062.1:c.604A=
ENST00000700065.1:n.2520A=
ENST00000700066.1:c.2024A=	ENSP00000514780.1:p.Gln675=
ENST00000281513.10:c.2507A= MANE Select	ENSP00000281513.5:p.Gln836=
ENST00000281513.9:c.2507A=	ENSP00000281513.5:p.Gln836=
ENST00000441755.5:c.8A=	ENSP00000396501.1:p.Gln3=
ENST00000442506.5:c.10A=
NM_015909.3:c.2507A=	NP_056993.2:p.Gln836=
NR_052013.2:n.2551A=
XM_011510357.1:c.2378A=	XP_011508659.1:p.Gln793=
XM_011510358.1:c.2507A=	XP_011508660.1:p.Gln836=
XM_011510359.1:c.1868A=	XP_011508661.1:p.Gln623=
XM_011510360.1:c.308A=	XP_011508662.1:p.Gln103=
XM_011510361.1:c.299A=	XP_011508663.1:p.Gln100=
XM_011510357.2:c.2378A=	XP_011508659.1:p.Gln793=
XM_011510358.2:c.2507A=	XP_011508660.1:p.Gln836=
XM_011510360.2:c.308A=	XP_011508662.1:p.Gln103=
XM_011510361.2:c.299A=	XP_011508663.1:p.Gln100=
XM_017004317.1:c.2507A=	XP_016859806.1:p.Gln836=
XM_024452961.1:c.1868A=	XP_024308729.1:p.Gln623=
NM_015909.4:c.2507A= MANE Select	NP_056993.2:p.Gln836=
NR_052013.3:n.2537A=