Canonical Allele Identifier: CA2490889330

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424389T= , CM000664.2:g.15424389T=	GRCh38
NC_000002.11:g.15564513T= , CM000664.1:g.15564513T=	GRCh37
NC_000002.10:g.15481964T=	NCBI36
NG_032964.1:g.141960A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.600A=
ENST00000700062.1:c.600A=
ENST00000700065.1:n.2516A=
ENST00000700066.1:c.2020A=	ENSP00000514780.1:p.Thr674=
ENST00000281513.10:c.2503A= MANE Select	ENSP00000281513.5:p.Thr835=
ENST00000281513.9:c.2503A=	ENSP00000281513.5:p.Thr835=
ENST00000441755.5:c.4A=	ENSP00000396501.1:p.Thr2=
ENST00000442506.5:c.6A=
NM_015909.3:c.2503A=	NP_056993.2:p.Thr835=
NR_052013.2:n.2547A=
XM_011510357.1:c.2374A=	XP_011508659.1:p.Thr792=
XM_011510358.1:c.2503A=	XP_011508660.1:p.Thr835=
XM_011510359.1:c.1864A=	XP_011508661.1:p.Thr622=
XM_011510360.1:c.304A=	XP_011508662.1:p.Thr102=
XM_011510361.1:c.295A=	XP_011508663.1:p.Thr99=
XM_011510357.2:c.2374A=	XP_011508659.1:p.Thr792=
XM_011510358.2:c.2503A=	XP_011508660.1:p.Thr835=
XM_011510360.2:c.304A=	XP_011508662.1:p.Thr102=
XM_011510361.2:c.295A=	XP_011508663.1:p.Thr99=
XM_017004317.1:c.2503A=	XP_016859806.1:p.Thr835=
XM_024452961.1:c.1864A=	XP_024308729.1:p.Thr622=
NM_015909.4:c.2503A= MANE Select	NP_056993.2:p.Thr835=
NR_052013.3:n.2533A=