Canonical Allele Identifier: CA2490796204
Gene: NBAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15218843T= , CM000664.2:g.15218843T= GRCh38
NC_000002.11:g.15358967T= , CM000664.1:g.15358967T= GRCh37
NC_000002.10:g.15276418T= NCBI36
NG_032964.1:g.347506A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.4348A=
ENST00000700062.1:c.4426+13579A=
ENST00000700063.1:c.873A=
ENST00000700064.1:c.2218A=
ENST00000281513.10:c.6362A= MANE Select ENSP00000281513.5:p.Glu2121=
ENST00000281513.9:c.6362A= ENSP00000281513.5:p.Glu2121=
ENST00000417461.5:c.512+13579A= ENSP00000392421.1:n.512+13579A=
ENST00000442506.5:c.3505A=
NM_015909.3:c.6362A= NP_056993.2:p.Glu2121=
NR_052013.2:n.6280+13579A=
XM_011510357.1:c.6233A= XP_011508659.1:p.Glu2078=
XM_011510358.1:c.6362A= XP_011508660.1:p.Glu2121=
XM_011510359.1:c.5723A= XP_011508661.1:p.Glu1908=
XM_011510360.1:c.4163A= XP_011508662.1:p.Glu1388=
XM_011510361.1:c.4154A= XP_011508663.1:p.Glu1385=
XM_011510357.2:c.6233A= XP_011508659.1:p.Glu2078=
XM_011510358.2:c.6362A= XP_011508660.1:p.Glu2121=
XM_011510360.2:c.4163A= XP_011508662.1:p.Glu1388=
XM_011510361.2:c.4154A= XP_011508663.1:p.Glu1385=
XM_017004317.1:c.6362A= XP_016859806.1:p.Glu2121=
XM_024452961.1:c.5723A= XP_024308729.1:p.Glu1908=
NM_015909.4:c.6362A= MANE Select NP_056993.2:p.Glu2121=
NR_052013.3:n.6266+13579A=