Canonical Allele Identifier: CA2490879591

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15402184G= , CM000664.2:g.15402184G=	GRCh38
NC_000002.11:g.15542308G= , CM000664.1:g.15542308G=	GRCh37
NC_000002.10:g.15459759G=	NCBI36
NG_032964.1:g.164165C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.1152C=
ENST00000700062.1:c.1152C=
ENST00000700065.1:n.3068C=
ENST00000281513.10:c.3055C= MANE Select	ENSP00000281513.5:p.Pro1019=
ENST00000281513.9:c.3055C=	ENSP00000281513.5:p.Pro1019=
ENST00000429842.1:c.347C=
ENST00000441755.5:c.196C=	ENSP00000396501.1:p.Pro66=
ENST00000442506.5:c.198C=
NM_015909.3:c.3055C=	NP_056993.2:p.Pro1019=
NR_052013.2:n.3099C=
XM_011510357.1:c.2926C=	XP_011508659.1:p.Pro976=
XM_011510358.1:c.3055C=	XP_011508660.1:p.Pro1019=
XM_011510359.1:c.2416C=	XP_011508661.1:p.Pro806=
XM_011510360.1:c.856C=	XP_011508662.1:p.Pro286=
XM_011510361.1:c.847C=	XP_011508663.1:p.Pro283=
XM_011510357.2:c.2926C=	XP_011508659.1:p.Pro976=
XM_011510358.2:c.3055C=	XP_011508660.1:p.Pro1019=
XM_011510360.2:c.856C=	XP_011508662.1:p.Pro286=
XM_011510361.2:c.847C=	XP_011508663.1:p.Pro283=
XM_017004317.1:c.3055C=	XP_016859806.1:p.Pro1019=
XM_024452961.1:c.2416C=	XP_024308729.1:p.Pro806=
NM_015909.4:c.3055C= MANE Select	NP_056993.2:p.Pro1019=
NR_052013.3:n.3085C=