Canonical Allele Identifier: CA2490879635

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15402300A= , CM000664.2:g.15402300A=	GRCh38
NC_000002.11:g.15542424A= , CM000664.1:g.15542424A=	GRCh37
NC_000002.10:g.15459875A=	NCBI36
NG_032964.1:g.164049T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700061.1:c.1036T=
ENST00000700062.1:c.1036T=
ENST00000700065.1:n.2952T=
ENST00000281513.10:c.2939T= MANE Select	ENSP00000281513.5:p.Leu980=
ENST00000281513.9:c.2939T=	ENSP00000281513.5:p.Leu980=
ENST00000429842.1:c.231T=
ENST00000441755.5:c.80T=	ENSP00000396501.1:p.Leu27=
ENST00000442506.5:c.82T=
NM_015909.3:c.2939T=	NP_056993.2:p.Leu980=
NR_052013.2:n.2983T=
XM_011510357.1:c.2810T=	XP_011508659.1:p.Leu937=
XM_011510358.1:c.2939T=	XP_011508660.1:p.Leu980=
XM_011510359.1:c.2300T=	XP_011508661.1:p.Leu767=
XM_011510360.1:c.740T=	XP_011508662.1:p.Leu247=
XM_011510361.1:c.731T=	XP_011508663.1:p.Leu244=
XM_011510357.2:c.2810T=	XP_011508659.1:p.Leu937=
XM_011510358.2:c.2939T=	XP_011508660.1:p.Leu980=
XM_011510360.2:c.740T=	XP_011508662.1:p.Leu247=
XM_011510361.2:c.731T=	XP_011508663.1:p.Leu244=
XM_017004317.1:c.2939T=	XP_016859806.1:p.Leu980=
XM_024452961.1:c.2300T=	XP_024308729.1:p.Leu767=
NM_015909.4:c.2939T= MANE Select	NP_056993.2:p.Leu980=
NR_052013.3:n.2969T=