Canonical Allele Identifier: CA2657911735
Gene: NBAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15402356del , CM000664.2:g.15402356del GRCh38
NC_000002.11:g.15542480del , CM000664.1:g.15542480del GRCh37
NC_000002.10:g.15459931del NCBI36
NG_032964.1:g.163997del

Transcript Alleles

HGVS Amino-acid change
ENST00000700061.1:c.1035-51del
ENST00000700062.1:c.1035-51del
ENST00000700065.1:n.2951-51del
ENST00000281513.10:c.2938-51del MANE Select ENSP00000281513.5:n.2938-51del
ENST00000281513.9:c.2938-51del ENSP00000281513.5:n.2938-51del
ENST00000429842.1:c.230-51del
ENST00000441755.5:c.79-51del ENSP00000396501.1:n.79-51del
ENST00000442506.5:c.81-51del
NM_015909.3:c.2938-51del NP_056993.2:n.2938-51del
NR_052013.2:n.2982-51del
XM_011510357.1:c.2809-51del XP_011508659.1:n.2809-51del
XM_011510358.1:c.2938-51del XP_011508660.1:n.2938-51del
XM_011510359.1:c.2299-51del XP_011508661.1:n.2299-51del
XM_011510360.1:c.739-51del XP_011508662.1:n.739-51del
XM_011510361.1:c.730-51del XP_011508663.1:n.730-51del
XM_011510357.2:c.2809-51del XP_011508659.1:n.2809-51del
XM_011510358.2:c.2938-51del XP_011508660.1:n.2938-51del
XM_011510360.2:c.739-51del XP_011508662.1:n.739-51del
XM_011510361.2:c.730-51del XP_011508663.1:n.730-51del
XM_017004317.1:c.2938-51del XP_016859806.1:n.2938-51del
XM_024452961.1:c.2299-51del XP_024308729.1:n.2299-51del
NM_015909.4:c.2938-51del MANE Select NP_056993.2:n.2938-51del
NR_052013.3:n.2968-51del