Canonical Allele Identifier: CA2657912215
Gene: NBAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15424564del , CM000664.2:g.15424564del GRCh38
NC_000002.11:g.15564688del , CM000664.1:g.15564688del GRCh37
NC_000002.10:g.15482139del NCBI36
NG_032964.1:g.141785del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.521-96del
ENST00000700062.1:c.521-96del
ENST00000700065.1:n.2437-96del
ENST00000700066.1:c.1941-96del ENSP00000514780.1:n.1941-96del
ENST00000281513.10:c.2424-96del MANE Select ENSP00000281513.5:n.2424-96del
ENST00000281513.9:c.2424-96del ENSP00000281513.5:n.2424-96del
NM_015909.3:c.2424-96del NP_056993.2:n.2424-96del
NR_052013.2:n.2468-96del
XM_011510357.1:c.2295-96del XP_011508659.1:n.2295-96del
XM_011510358.1:c.2424-96del XP_011508660.1:n.2424-96del
XM_011510359.1:c.1785-96del XP_011508661.1:n.1785-96del
XM_011510360.1:c.225-96del XP_011508662.1:n.225-96del
XM_011510361.1:c.216-96del XP_011508663.1:n.216-96del
XM_011510357.2:c.2295-96del XP_011508659.1:n.2295-96del
XM_011510358.2:c.2424-96del XP_011508660.1:n.2424-96del
XM_011510360.2:c.225-96del XP_011508662.1:n.225-96del
XM_011510361.2:c.216-96del XP_011508663.1:n.216-96del
XM_017004317.1:c.2424-96del XP_016859806.1:n.2424-96del
XM_024452961.1:c.1785-96del XP_024308729.1:n.1785-96del
NM_015909.4:c.2424-96del MANE Select NP_056993.2:n.2424-96del
NR_052013.3:n.2454-96del