Canonical Allele Identifier: CA2490889339

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424401T= , CM000664.2:g.15424401T=	GRCh38
NC_000002.11:g.15564525T= , CM000664.1:g.15564525T=	GRCh37
NC_000002.10:g.15481976T=	NCBI36
NG_032964.1:g.141948A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.588A=
ENST00000700062.1:c.588A=
ENST00000700065.1:n.2504A=
ENST00000700066.1:c.2008A=	ENSP00000514780.1:p.Arg670=
ENST00000281513.10:c.2491A= MANE Select	ENSP00000281513.5:p.Arg831=
ENST00000281513.9:c.2491A=	ENSP00000281513.5:p.Arg831=
NM_015909.3:c.2491A=	NP_056993.2:p.Arg831=
NR_052013.2:n.2535A=
XM_011510357.1:c.2362A=	XP_011508659.1:p.Arg788=
XM_011510358.1:c.2491A=	XP_011508660.1:p.Arg831=
XM_011510359.1:c.1852A=	XP_011508661.1:p.Arg618=
XM_011510360.1:c.292A=	XP_011508662.1:p.Arg98=
XM_011510361.1:c.283A=	XP_011508663.1:p.Arg95=
XM_011510357.2:c.2362A=	XP_011508659.1:p.Arg788=
XM_011510358.2:c.2491A=	XP_011508660.1:p.Arg831=
XM_011510360.2:c.292A=	XP_011508662.1:p.Arg98=
XM_011510361.2:c.283A=	XP_011508663.1:p.Arg95=
XM_017004317.1:c.2491A=	XP_016859806.1:p.Arg831=
XM_024452961.1:c.1852A=	XP_024308729.1:p.Arg618=
NM_015909.4:c.2491A= MANE Select	NP_056993.2:p.Arg831=
NR_052013.3:n.2521A=