Canonical Allele Identifier: CA2490879629

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15402280C= , CM000664.2:g.15402280C=	GRCh38
NC_000002.11:g.15542404C= , CM000664.1:g.15542404C=	GRCh37
NC_000002.10:g.15459855C=	NCBI36
NG_032964.1:g.164069G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.1056G=
ENST00000700062.1:c.1056G=
ENST00000700065.1:n.2972G=
ENST00000281513.10:c.2959G= MANE Select	ENSP00000281513.5:p.Asp987=
ENST00000281513.9:c.2959G=	ENSP00000281513.5:p.Asp987=
ENST00000429842.1:c.251G=
ENST00000441755.5:c.100G=	ENSP00000396501.1:p.Asp34=
ENST00000442506.5:c.102G=
NM_015909.3:c.2959G=	NP_056993.2:p.Asp987=
NR_052013.2:n.3003G=
XM_011510357.1:c.2830G=	XP_011508659.1:p.Asp944=
XM_011510358.1:c.2959G=	XP_011508660.1:p.Asp987=
XM_011510359.1:c.2320G=	XP_011508661.1:p.Asp774=
XM_011510360.1:c.760G=	XP_011508662.1:p.Asp254=
XM_011510361.1:c.751G=	XP_011508663.1:p.Asp251=
XM_011510357.2:c.2830G=	XP_011508659.1:p.Asp944=
XM_011510358.2:c.2959G=	XP_011508660.1:p.Asp987=
XM_011510360.2:c.760G=	XP_011508662.1:p.Asp254=
XM_011510361.2:c.751G=	XP_011508663.1:p.Asp251=
XM_017004317.1:c.2959G=	XP_016859806.1:p.Asp987=
XM_024452961.1:c.2320G=	XP_024308729.1:p.Asp774=
NM_015909.4:c.2959G= MANE Select	NP_056993.2:p.Asp987=
NR_052013.3:n.2989G=