Canonical Allele Identifier: CA2490889363
Gene: NBAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15424466A= , CM000664.2:g.15424466A= GRCh38
NC_000002.11:g.15564590A= , CM000664.1:g.15564590A= GRCh37
NC_000002.10:g.15482041A= NCBI36
NG_032964.1:g.141883T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.523T=
ENST00000700062.1:c.523T=
ENST00000700065.1:n.2439T=
ENST00000700066.1:c.1943T= ENSP00000514780.1:p.Met648=
ENST00000281513.10:c.2426T= MANE Select ENSP00000281513.5:p.Met809=
ENST00000281513.9:c.2426T= ENSP00000281513.5:p.Met809=
NM_015909.3:c.2426T= NP_056993.2:p.Met809=
NR_052013.2:n.2470T=
XM_011510357.1:c.2297T= XP_011508659.1:p.Met766=
XM_011510358.1:c.2426T= XP_011508660.1:p.Met809=
XM_011510359.1:c.1787T= XP_011508661.1:p.Met596=
XM_011510360.1:c.227T= XP_011508662.1:p.Met76=
XM_011510361.1:c.218T= XP_011508663.1:p.Met73=
XM_011510357.2:c.2297T= XP_011508659.1:p.Met766=
XM_011510358.2:c.2426T= XP_011508660.1:p.Met809=
XM_011510360.2:c.227T= XP_011508662.1:p.Met76=
XM_011510361.2:c.218T= XP_011508663.1:p.Met73=
XM_017004317.1:c.2426T= XP_016859806.1:p.Met809=
XM_024452961.1:c.1787T= XP_024308729.1:p.Met596=
NM_015909.4:c.2426T= MANE Select NP_056993.2:p.Met809=
NR_052013.3:n.2456T=