Canonical Allele Identifier: CA2490889351
Gene: NBAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15424433T= , CM000664.2:g.15424433T= GRCh38
NC_000002.11:g.15564557T= , CM000664.1:g.15564557T= GRCh37
NC_000002.10:g.15482008T= NCBI36
NG_032964.1:g.141916A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.556A=
ENST00000700062.1:c.556A=
ENST00000700065.1:n.2472A=
ENST00000700066.1:c.1976A= ENSP00000514780.1:p.Glu659=
ENST00000281513.10:c.2459A= MANE Select ENSP00000281513.5:p.Glu820=
ENST00000281513.9:c.2459A= ENSP00000281513.5:p.Glu820=
NM_015909.3:c.2459A= NP_056993.2:p.Glu820=
NR_052013.2:n.2503A=
XM_011510357.1:c.2330A= XP_011508659.1:p.Glu777=
XM_011510358.1:c.2459A= XP_011508660.1:p.Glu820=
XM_011510359.1:c.1820A= XP_011508661.1:p.Glu607=
XM_011510360.1:c.260A= XP_011508662.1:p.Glu87=
XM_011510361.1:c.251A= XP_011508663.1:p.Glu84=
XM_011510357.2:c.2330A= XP_011508659.1:p.Glu777=
XM_011510358.2:c.2459A= XP_011508660.1:p.Glu820=
XM_011510360.2:c.260A= XP_011508662.1:p.Glu87=
XM_011510361.2:c.251A= XP_011508663.1:p.Glu84=
XM_017004317.1:c.2459A= XP_016859806.1:p.Glu820=
XM_024452961.1:c.1820A= XP_024308729.1:p.Glu607=
NM_015909.4:c.2459A= MANE Select NP_056993.2:p.Glu820=
NR_052013.3:n.2489A=