Canonical Allele Identifier: CA2490796311
Gene: NBAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15219030T= , CM000664.2:g.15219030T= GRCh38
NC_000002.11:g.15359154T= , CM000664.1:g.15359154T= GRCh37
NC_000002.10:g.15276605T= NCBI36
NG_032964.1:g.347319A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.4223-62A=
ENST00000700062.1:c.4426+13392A=
ENST00000700063.1:c.748-62A=
ENST00000700064.1:c.2093-62A=
ENST00000281513.10:c.6237-62A= MANE Select ENSP00000281513.5:n.6237-62A=
ENST00000281513.9:c.6237-62A= ENSP00000281513.5:n.6237-62A=
ENST00000417461.5:c.512+13392A= ENSP00000392421.1:n.512+13392A=
ENST00000442506.5:c.3380-62A=
NM_015909.3:c.6237-62A= NP_056993.2:n.6237-62A=
NR_052013.2:n.6280+13392A=
XM_011510357.1:c.6108-62A= XP_011508659.1:n.6108-62A=
XM_011510358.1:c.6237-62A= XP_011508660.1:n.6237-62A=
XM_011510359.1:c.5598-62A= XP_011508661.1:n.5598-62A=
XM_011510360.1:c.4038-62A= XP_011508662.1:n.4038-62A=
XM_011510361.1:c.4029-62A= XP_011508663.1:n.4029-62A=
XM_011510357.2:c.6108-62A= XP_011508659.1:n.6108-62A=
XM_011510358.2:c.6237-62A= XP_011508660.1:n.6237-62A=
XM_011510360.2:c.4038-62A= XP_011508662.1:n.4038-62A=
XM_011510361.2:c.4029-62A= XP_011508663.1:n.4029-62A=
XM_017004317.1:c.6237-62A= XP_016859806.1:n.6237-62A=
XM_024452961.1:c.5598-62A= XP_024308729.1:n.5598-62A=
NM_015909.4:c.6237-62A= MANE Select NP_056993.2:n.6237-62A=
NR_052013.3:n.6266+13392A=