Canonical Allele Identifier: CA2490879596

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15402195A= , CM000664.2:g.15402195A=	GRCh38
NC_000002.11:g.15542319A= , CM000664.1:g.15542319A=	GRCh37
NC_000002.10:g.15459770A=	NCBI36
NG_032964.1:g.164154T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.1141T=
ENST00000700062.1:c.1141T=
ENST00000700065.1:n.3057T=
ENST00000281513.10:c.3044T= MANE Select	ENSP00000281513.5:p.Leu1015=
ENST00000281513.9:c.3044T=	ENSP00000281513.5:p.Leu1015=
ENST00000429842.1:c.336T=
ENST00000441755.5:c.185T=	ENSP00000396501.1:p.Leu62=
ENST00000442506.5:c.187T=
NM_015909.3:c.3044T=	NP_056993.2:p.Leu1015=
NR_052013.2:n.3088T=
XM_011510357.1:c.2915T=	XP_011508659.1:p.Leu972=
XM_011510358.1:c.3044T=	XP_011508660.1:p.Leu1015=
XM_011510359.1:c.2405T=	XP_011508661.1:p.Leu802=
XM_011510360.1:c.845T=	XP_011508662.1:p.Leu282=
XM_011510361.1:c.836T=	XP_011508663.1:p.Leu279=
XM_011510357.2:c.2915T=	XP_011508659.1:p.Leu972=
XM_011510358.2:c.3044T=	XP_011508660.1:p.Leu1015=
XM_011510360.2:c.845T=	XP_011508662.1:p.Leu282=
XM_011510361.2:c.836T=	XP_011508663.1:p.Leu279=
XM_017004317.1:c.3044T=	XP_016859806.1:p.Leu1015=
XM_024452961.1:c.2405T=	XP_024308729.1:p.Leu802=
NM_015909.4:c.3044T= MANE Select	NP_056993.2:p.Leu1015=
NR_052013.3:n.3074T=