Canonical Allele Identifier: CA2490796218

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218866C= , CM000664.2:g.15218866C=	GRCh38
NC_000002.11:g.15358990C= , CM000664.1:g.15358990C=	GRCh37
NC_000002.10:g.15276441C=	NCBI36
NG_032964.1:g.347483G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4325G=
ENST00000700062.1:c.4426+13556G=
ENST00000700063.1:c.850G=
ENST00000700064.1:c.2195G=
ENST00000281513.10:c.6339G= MANE Select	ENSP00000281513.5:p.Leu2113=
ENST00000281513.9:c.6339G=	ENSP00000281513.5:p.Leu2113=
ENST00000417461.5:c.512+13556G=	ENSP00000392421.1:n.512+13556G=
ENST00000442506.5:c.3482G=
NM_015909.3:c.6339G=	NP_056993.2:p.Leu2113=
NR_052013.2:n.6280+13556G=
XM_011510357.1:c.6210G=	XP_011508659.1:p.Leu2070=
XM_011510358.1:c.6339G=	XP_011508660.1:p.Leu2113=
XM_011510359.1:c.5700G=	XP_011508661.1:p.Leu1900=
XM_011510360.1:c.4140G=	XP_011508662.1:p.Leu1380=
XM_011510361.1:c.4131G=	XP_011508663.1:p.Leu1377=
XM_011510357.2:c.6210G=	XP_011508659.1:p.Leu2070=
XM_011510358.2:c.6339G=	XP_011508660.1:p.Leu2113=
XM_011510360.2:c.4140G=	XP_011508662.1:p.Leu1380=
XM_011510361.2:c.4131G=	XP_011508663.1:p.Leu1377=
XM_017004317.1:c.6339G=	XP_016859806.1:p.Leu2113=
XM_024452961.1:c.5700G=	XP_024308729.1:p.Leu1900=
NM_015909.4:c.6339G= MANE Select	NP_056993.2:p.Leu2113=
NR_052013.3:n.6266+13556G=