Canonical Allele Identifier: CA2490796205

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218845A= , CM000664.2:g.15218845A=	GRCh38
NC_000002.11:g.15358969A= , CM000664.1:g.15358969A=	GRCh37
NC_000002.10:g.15276420A=	NCBI36
NG_032964.1:g.347504T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4346T=
ENST00000700062.1:c.4426+13577T=
ENST00000700063.1:c.871T=
ENST00000700064.1:c.2216T=
ENST00000281513.10:c.6360T= MANE Select	ENSP00000281513.5:p.Thr2120=
ENST00000281513.9:c.6360T=	ENSP00000281513.5:p.Thr2120=
ENST00000417461.5:c.512+13577T=	ENSP00000392421.1:n.512+13577T=
ENST00000442506.5:c.3503T=
NM_015909.3:c.6360T=	NP_056993.2:p.Thr2120=
NR_052013.2:n.6280+13577T=
XM_011510357.1:c.6231T=	XP_011508659.1:p.Thr2077=
XM_011510358.1:c.6360T=	XP_011508660.1:p.Thr2120=
XM_011510359.1:c.5721T=	XP_011508661.1:p.Thr1907=
XM_011510360.1:c.4161T=	XP_011508662.1:p.Thr1387=
XM_011510361.1:c.4152T=	XP_011508663.1:p.Thr1384=
XM_011510357.2:c.6231T=	XP_011508659.1:p.Thr2077=
XM_011510358.2:c.6360T=	XP_011508660.1:p.Thr2120=
XM_011510360.2:c.4161T=	XP_011508662.1:p.Thr1387=
XM_011510361.2:c.4152T=	XP_011508663.1:p.Thr1384=
XM_017004317.1:c.6360T=	XP_016859806.1:p.Thr2120=
XM_024452961.1:c.5721T=	XP_024308729.1:p.Thr1907=
NM_015909.4:c.6360T= MANE Select	NP_056993.2:p.Thr2120=
NR_052013.3:n.6266+13577T=