Canonical Allele Identifier: CA2490879600
Gene: NBAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15402207C= , CM000664.2:g.15402207C= GRCh38
NC_000002.11:g.15542331C= , CM000664.1:g.15542331C= GRCh37
NC_000002.10:g.15459782C= NCBI36
NG_032964.1:g.164142G=

Transcript Alleles

HGVS Amino-acid change
ENST00000700061.1:c.1129G=
ENST00000700062.1:c.1129G=
ENST00000700065.1:n.3045G=
ENST00000281513.10:c.3032G= MANE Select ENSP00000281513.5:p.Cys1011=
ENST00000281513.9:c.3032G= ENSP00000281513.5:p.Cys1011=
ENST00000429842.1:c.324G=
ENST00000441755.5:c.173G= ENSP00000396501.1:p.Cys58=
ENST00000442506.5:c.175G=
NM_015909.3:c.3032G= NP_056993.2:p.Cys1011=
NR_052013.2:n.3076G=
XM_011510357.1:c.2903G= XP_011508659.1:p.Cys968=
XM_011510358.1:c.3032G= XP_011508660.1:p.Cys1011=
XM_011510359.1:c.2393G= XP_011508661.1:p.Cys798=
XM_011510360.1:c.833G= XP_011508662.1:p.Cys278=
XM_011510361.1:c.824G= XP_011508663.1:p.Cys275=
XM_011510357.2:c.2903G= XP_011508659.1:p.Cys968=
XM_011510358.2:c.3032G= XP_011508660.1:p.Cys1011=
XM_011510360.2:c.833G= XP_011508662.1:p.Cys278=
XM_011510361.2:c.824G= XP_011508663.1:p.Cys275=
XM_017004317.1:c.3032G= XP_016859806.1:p.Cys1011=
XM_024452961.1:c.2393G= XP_024308729.1:p.Cys798=
NM_015909.4:c.3032G= MANE Select NP_056993.2:p.Cys1011=
NR_052013.3:n.3062G=