Canonical Allele Identifier: CA2490889299

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424327A= , CM000664.2:g.15424327A=	GRCh38
NC_000002.11:g.15564451A= , CM000664.1:g.15564451A=	GRCh37
NC_000002.10:g.15481902A=	NCBI36
NG_032964.1:g.142022T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.662T=
ENST00000700062.1:c.662T=
ENST00000700065.1:n.2578T=
ENST00000700066.1:c.2082T=	ENSP00000514780.1:p.His694=
ENST00000281513.10:c.2565T= MANE Select	ENSP00000281513.5:p.His855=
ENST00000281513.9:c.2565T=	ENSP00000281513.5:p.His855=
ENST00000441755.5:c.66T=	ENSP00000396501.1:p.His22=
ENST00000442506.5:c.68T=
NM_015909.3:c.2565T=	NP_056993.2:p.His855=
NR_052013.2:n.2609T=
XM_011510357.1:c.2436T=	XP_011508659.1:p.His812=
XM_011510358.1:c.2565T=	XP_011508660.1:p.His855=
XM_011510359.1:c.1926T=	XP_011508661.1:p.His642=
XM_011510360.1:c.366T=	XP_011508662.1:p.His122=
XM_011510361.1:c.357T=	XP_011508663.1:p.His119=
XM_011510357.2:c.2436T=	XP_011508659.1:p.His812=
XM_011510358.2:c.2565T=	XP_011508660.1:p.His855=
XM_011510360.2:c.366T=	XP_011508662.1:p.His122=
XM_011510361.2:c.357T=	XP_011508663.1:p.His119=
XM_017004317.1:c.2565T=	XP_016859806.1:p.His855=
XM_024452961.1:c.1926T=	XP_024308729.1:p.His642=
NM_015909.4:c.2565T= MANE Select	NP_056993.2:p.His855=
NR_052013.3:n.2595T=