Canonical Allele Identifier: CA2490796292
Gene: NBAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15219006A= , CM000664.2:g.15219006A= GRCh38
NC_000002.11:g.15359130A= , CM000664.1:g.15359130A= GRCh37
NC_000002.10:g.15276581A= NCBI36
NG_032964.1:g.347343T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.4223-38T=
ENST00000700062.1:c.4426+13416T=
ENST00000700063.1:c.748-38T=
ENST00000700064.1:c.2093-38T=
ENST00000281513.10:c.6237-38T= MANE Select ENSP00000281513.5:n.6237-38T=
ENST00000281513.9:c.6237-38T= ENSP00000281513.5:n.6237-38T=
ENST00000417461.5:c.512+13416T= ENSP00000392421.1:n.512+13416T=
ENST00000442506.5:c.3380-38T=
NM_015909.3:c.6237-38T= NP_056993.2:n.6237-38T=
NR_052013.2:n.6280+13416T=
XM_011510357.1:c.6108-38T= XP_011508659.1:n.6108-38T=
XM_011510358.1:c.6237-38T= XP_011508660.1:n.6237-38T=
XM_011510359.1:c.5598-38T= XP_011508661.1:n.5598-38T=
XM_011510360.1:c.4038-38T= XP_011508662.1:n.4038-38T=
XM_011510361.1:c.4029-38T= XP_011508663.1:n.4029-38T=
XM_011510357.2:c.6108-38T= XP_011508659.1:n.6108-38T=
XM_011510358.2:c.6237-38T= XP_011508660.1:n.6237-38T=
XM_011510360.2:c.4038-38T= XP_011508662.1:n.4038-38T=
XM_011510361.2:c.4029-38T= XP_011508663.1:n.4029-38T=
XM_017004317.1:c.6237-38T= XP_016859806.1:n.6237-38T=
XM_024452961.1:c.5598-38T= XP_024308729.1:n.5598-38T=
NM_015909.4:c.6237-38T= MANE Select NP_056993.2:n.6237-38T=
NR_052013.3:n.6266+13416T=