Canonical Allele Identifier: CA345884697
Gene: NBAS HGNC NCBI

Linked Data

dbSNP Id: rs1666781798

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15218886T>C , CM000664.2:g.15218886T>C GRCh38
NC_000002.11:g.15359010T>C , CM000664.1:g.15359010T>C GRCh37
NC_000002.10:g.15276461T>C NCBI36
NG_032964.1:g.347463A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.4305A>G
ENST00000700062.1:c.4426+13536A>G
ENST00000700063.1:c.830A>G
ENST00000700064.1:c.2175A>G
ENST00000281513.10:c.6319A>G MANE Select ENSP00000281513.5:p.Ile2107Val
ENST00000281513.9:c.6319A>G ENSP00000281513.5:p.Ile2107Val
ENST00000417461.5:c.512+13536A>G ENSP00000392421.1:n.512+13536A>G
ENST00000442506.5:c.3462A>G
NM_015909.3:c.6319A>G NP_056993.2:p.Ile2107Val
NR_052013.2:n.6280+13536A>G
XM_011510357.1:c.6190A>G XP_011508659.1:p.Ile2064Val
XM_011510358.1:c.6319A>G XP_011508660.1:p.Ile2107Val
XM_011510359.1:c.5680A>G XP_011508661.1:p.Ile1894Val
XM_011510360.1:c.4120A>G XP_011508662.1:p.Ile1374Val
XM_011510361.1:c.4111A>G XP_011508663.1:p.Ile1371Val
XM_011510357.2:c.6190A>G XP_011508659.1:p.Ile2064Val
XM_011510358.2:c.6319A>G XP_011508660.1:p.Ile2107Val
XM_011510360.2:c.4120A>G XP_011508662.1:p.Ile1374Val
XM_011510361.2:c.4111A>G XP_011508663.1:p.Ile1371Val
XM_017004317.1:c.6319A>G XP_016859806.1:p.Ile2107Val
XM_024452961.1:c.5680A>G XP_024308729.1:p.Ile1894Val
NM_015909.4:c.6319A>G MANE Select NP_056993.2:p.Ile2107Val
NR_052013.3:n.6266+13536A>G