Canonical Allele Identifier: CA2490935307

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15524632C= , CM000664.2:g.15524632C=	GRCh38
NC_000002.11:g.15664756C= , CM000664.1:g.15664756C=	GRCh37
NC_000002.10:g.15582207C=	NCBI36
NG_032964.1:g.41717G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700065.1:n.759+9911G=
ENST00000700066.1:c.263+9911G=	ENSP00000514780.1:n.263+9911G=
ENST00000700067.1:n.761+9911G=
ENST00000700068.1:n.761+9911G=
ENST00000700069.1:c.746+9911G=	ENSP00000514781.1:n.746+9911G=
ENST00000700070.1:c.*405+9911G=	ENSP00000514782.1:n.*405+9911G=
ENST00000700071.1:n.777-9401G=
ENST00000281513.10:c.746+9911G= MANE Select	ENSP00000281513.5:n.746+9911G=
ENST00000281513.9:c.746+9911G=	ENSP00000281513.5:n.746+9911G=
NM_015909.3:c.746+9911G=	NP_056993.2:n.746+9911G=
NR_052013.2:n.790+9911G=
XM_011510357.1:c.746+9911G=	XP_011508659.1:n.746+9911G=
XM_011510358.1:c.746+9911G=	XP_011508660.1:n.746+9911G=
XM_011510359.1:c.107+9911G=	XP_011508661.1:n.107+9911G=
XM_011510357.2:c.746+9911G=	XP_011508659.1:n.746+9911G=
XM_011510358.2:c.746+9911G=	XP_011508660.1:n.746+9911G=
XM_017004317.1:c.746+9911G=	XP_016859806.1:n.746+9911G=
XM_024452961.1:c.107+9911G=	XP_024308729.1:n.107+9911G=
NM_015909.4:c.746+9911G= MANE Select	NP_056993.2:n.746+9911G=
NR_052013.3:n.776+9911G=