Canonical Allele Identifier: CA2490889355
Gene: NBAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15424441A= , CM000664.2:g.15424441A= GRCh38
NC_000002.11:g.15564565A= , CM000664.1:g.15564565A= GRCh37
NC_000002.10:g.15482016A= NCBI36
NG_032964.1:g.141908T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.548T=
ENST00000700062.1:c.548T=
ENST00000700065.1:n.2464T=
ENST00000700066.1:c.1968T= ENSP00000514780.1:p.Asp656=
ENST00000281513.10:c.2451T= MANE Select ENSP00000281513.5:p.Asp817=
ENST00000281513.9:c.2451T= ENSP00000281513.5:p.Asp817=
NM_015909.3:c.2451T= NP_056993.2:p.Asp817=
NR_052013.2:n.2495T=
XM_011510357.1:c.2322T= XP_011508659.1:p.Asp774=
XM_011510358.1:c.2451T= XP_011508660.1:p.Asp817=
XM_011510359.1:c.1812T= XP_011508661.1:p.Asp604=
XM_011510360.1:c.252T= XP_011508662.1:p.Asp84=
XM_011510361.1:c.243T= XP_011508663.1:p.Asp81=
XM_011510357.2:c.2322T= XP_011508659.1:p.Asp774=
XM_011510358.2:c.2451T= XP_011508660.1:p.Asp817=
XM_011510360.2:c.252T= XP_011508662.1:p.Asp84=
XM_011510361.2:c.243T= XP_011508663.1:p.Asp81=
XM_017004317.1:c.2451T= XP_016859806.1:p.Asp817=
XM_024452961.1:c.1812T= XP_024308729.1:p.Asp604=
NM_015909.4:c.2451T= MANE Select NP_056993.2:p.Asp817=
NR_052013.3:n.2481T=