Canonical Allele Identifier: CA2490879633

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15402295G= , CM000664.2:g.15402295G=	GRCh38
NC_000002.11:g.15542419G= , CM000664.1:g.15542419G=	GRCh37
NC_000002.10:g.15459870G=	NCBI36
NG_032964.1:g.164054C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000700061.1:c.1041C=
ENST00000700062.1:c.1041C=
ENST00000700065.1:n.2957C=
ENST00000281513.10:c.2944C= MANE Select	ENSP00000281513.5:p.Gln982=
ENST00000281513.9:c.2944C=	ENSP00000281513.5:p.Gln982=
ENST00000429842.1:c.236C=
ENST00000441755.5:c.85C=	ENSP00000396501.1:p.Gln29=
ENST00000442506.5:c.87C=
NM_015909.3:c.2944C=	NP_056993.2:p.Gln982=
NR_052013.2:n.2988C=
XM_011510357.1:c.2815C=	XP_011508659.1:p.Gln939=
XM_011510358.1:c.2944C=	XP_011508660.1:p.Gln982=
XM_011510359.1:c.2305C=	XP_011508661.1:p.Gln769=
XM_011510360.1:c.745C=	XP_011508662.1:p.Gln249=
XM_011510361.1:c.736C=	XP_011508663.1:p.Gln246=
XM_011510357.2:c.2815C=	XP_011508659.1:p.Gln939=
XM_011510358.2:c.2944C=	XP_011508660.1:p.Gln982=
XM_011510360.2:c.745C=	XP_011508662.1:p.Gln249=
XM_011510361.2:c.736C=	XP_011508663.1:p.Gln246=
XM_017004317.1:c.2944C=	XP_016859806.1:p.Gln982=
XM_024452961.1:c.2305C=	XP_024308729.1:p.Gln769=
NM_015909.4:c.2944C= MANE Select	NP_056993.2:p.Gln982=
NR_052013.3:n.2974C=