Canonical Allele Identifier: CA2490889441
Gene: NBAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15424619C= , CM000664.2:g.15424619C= GRCh38
NC_000002.11:g.15564743C= , CM000664.1:g.15564743C= GRCh37
NC_000002.10:g.15482194C= NCBI36
NG_032964.1:g.141730G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.521-151G=
ENST00000700062.1:c.521-151G=
ENST00000700065.1:n.2437-151G=
ENST00000700066.1:c.1941-151G= ENSP00000514780.1:n.1941-151G=
ENST00000281513.10:c.2424-151G= MANE Select ENSP00000281513.5:n.2424-151G=
ENST00000281513.9:c.2424-151G= ENSP00000281513.5:n.2424-151G=
NM_015909.3:c.2424-151G= NP_056993.2:n.2424-151G=
NR_052013.2:n.2468-151G=
XM_011510357.1:c.2295-151G= XP_011508659.1:n.2295-151G=
XM_011510358.1:c.2424-151G= XP_011508660.1:n.2424-151G=
XM_011510359.1:c.1785-151G= XP_011508661.1:n.1785-151G=
XM_011510360.1:c.225-151G= XP_011508662.1:n.225-151G=
XM_011510361.1:c.216-151G= XP_011508663.1:n.216-151G=
XM_011510357.2:c.2295-151G= XP_011508659.1:n.2295-151G=
XM_011510358.2:c.2424-151G= XP_011508660.1:n.2424-151G=
XM_011510360.2:c.225-151G= XP_011508662.1:n.225-151G=
XM_011510361.2:c.216-151G= XP_011508663.1:n.216-151G=
XM_017004317.1:c.2424-151G= XP_016859806.1:n.2424-151G=
XM_024452961.1:c.1785-151G= XP_024308729.1:n.1785-151G=
NM_015909.4:c.2424-151G= MANE Select NP_056993.2:n.2424-151G=
NR_052013.3:n.2454-151G=