Canonical Allele Identifier: CA2490879568

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15402139A= , CM000664.2:g.15402139A=	GRCh38
NC_000002.11:g.15542263A= , CM000664.1:g.15542263A=	GRCh37
NC_000002.10:g.15459714A=	NCBI36
NG_032964.1:g.164210T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.1168+29T=
ENST00000700062.1:c.1168+29T=
ENST00000700065.1:n.3084+29T=
ENST00000281513.10:c.3071+29T= MANE Select	ENSP00000281513.5:n.3071+29T=
ENST00000281513.9:c.3071+29T=	ENSP00000281513.5:n.3071+29T=
ENST00000429842.1:c.363+29T=
ENST00000441755.5:c.212+29T=	ENSP00000396501.1:n.212+29T=
ENST00000442506.5:c.214+29T=
NM_015909.3:c.3071+29T=	NP_056993.2:n.3071+29T=
NR_052013.2:n.3115+29T=
XM_011510357.1:c.2942+29T=	XP_011508659.1:n.2942+29T=
XM_011510358.1:c.3071+29T=	XP_011508660.1:n.3071+29T=
XM_011510359.1:c.2432+29T=	XP_011508661.1:n.2432+29T=
XM_011510360.1:c.872+29T=	XP_011508662.1:n.872+29T=
XM_011510361.1:c.863+29T=	XP_011508663.1:n.863+29T=
XM_011510357.2:c.2942+29T=	XP_011508659.1:n.2942+29T=
XM_011510358.2:c.3071+29T=	XP_011508660.1:n.3071+29T=
XM_011510360.2:c.872+29T=	XP_011508662.1:n.872+29T=
XM_011510361.2:c.863+29T=	XP_011508663.1:n.863+29T=
XM_017004317.1:c.3071+29T=	XP_016859806.1:n.3071+29T=
XM_024452961.1:c.2432+29T=	XP_024308729.1:n.2432+29T=
NM_015909.4:c.3071+29T= MANE Select	NP_056993.2:n.3071+29T=
NR_052013.3:n.3101+29T=