Canonical Allele Identifier: CA2490889168

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424042G= , CM000664.2:g.15424042G=	GRCh38
NC_000002.11:g.15564166G= , CM000664.1:g.15564166G=	GRCh37
NC_000002.10:g.15481617G=	NCBI36
NG_032964.1:g.142307C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.674+273C=
ENST00000700062.1:c.674+273C=
ENST00000700065.1:n.2590+273C=
ENST00000700066.1:c.2094+273C=	ENSP00000514780.1:n.2094+273C=
ENST00000281513.10:c.2577+273C= MANE Select	ENSP00000281513.5:n.2577+273C=
ENST00000281513.9:c.2577+273C=	ENSP00000281513.5:n.2577+273C=
ENST00000441755.5:c.78+273C=	ENSP00000396501.1:n.78+273C=
ENST00000442506.5:c.80+273C=
NM_015909.3:c.2577+273C=	NP_056993.2:n.2577+273C=
NR_052013.2:n.2621+273C=
XM_011510357.1:c.2448+273C=	XP_011508659.1:n.2448+273C=
XM_011510358.1:c.2577+273C=	XP_011508660.1:n.2577+273C=
XM_011510359.1:c.1938+273C=	XP_011508661.1:n.1938+273C=
XM_011510360.1:c.378+273C=	XP_011508662.1:n.378+273C=
XM_011510361.1:c.369+273C=	XP_011508663.1:n.369+273C=
XM_011510357.2:c.2448+273C=	XP_011508659.1:n.2448+273C=
XM_011510358.2:c.2577+273C=	XP_011508660.1:n.2577+273C=
XM_011510360.2:c.378+273C=	XP_011508662.1:n.378+273C=
XM_011510361.2:c.369+273C=	XP_011508663.1:n.369+273C=
XM_017004317.1:c.2577+273C=	XP_016859806.1:n.2577+273C=
XM_024452961.1:c.1938+273C=	XP_024308729.1:n.1938+273C=
NM_015909.4:c.2577+273C= MANE Select	NP_056993.2:n.2577+273C=
NR_052013.3:n.2607+273C=