Canonical Allele Identifier: CA2657912192
Gene: NBAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15424541_15424544del , CM000664.2:g.15424541_15424544del GRCh38
NC_000002.11:g.15564665_15564668del , CM000664.1:g.15564665_15564668del GRCh37
NC_000002.10:g.15482116_15482119del NCBI36
NG_032964.1:g.141807_141810del

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.521-74_521-71del
ENST00000700062.1:c.521-74_521-71del
ENST00000700065.1:n.2437-74_2437-71del
ENST00000700066.1:c.1941-74_1941-71del ENSP00000514780.1:n.1941-74_1941-71del
ENST00000281513.10:c.2424-74_2424-71del MANE Select ENSP00000281513.5:n.2424-74_2424-71del
ENST00000281513.9:c.2424-74_2424-71del ENSP00000281513.5:n.2424-74_2424-71del
NM_015909.3:c.2424-74_2424-71del NP_056993.2:n.2424-74_2424-71del
NR_052013.2:n.2468-74_2468-71del
XM_011510357.1:c.2295-74_2295-71del XP_011508659.1:n.2295-74_2295-71del
XM_011510358.1:c.2424-74_2424-71del XP_011508660.1:n.2424-74_2424-71del
XM_011510359.1:c.1785-74_1785-71del XP_011508661.1:n.1785-74_1785-71del
XM_011510360.1:c.225-74_225-71del XP_011508662.1:n.225-74_225-71del
XM_011510361.1:c.216-74_216-71del XP_011508663.1:n.216-74_216-71del
XM_011510357.2:c.2295-74_2295-71del XP_011508659.1:n.2295-74_2295-71del
XM_011510358.2:c.2424-74_2424-71del XP_011508660.1:n.2424-74_2424-71del
XM_011510360.2:c.225-74_225-71del XP_011508662.1:n.225-74_225-71del
XM_011510361.2:c.216-74_216-71del XP_011508663.1:n.216-74_216-71del
XM_017004317.1:c.2424-74_2424-71del XP_016859806.1:n.2424-74_2424-71del
XM_024452961.1:c.1785-74_1785-71del XP_024308729.1:n.1785-74_1785-71del
NM_015909.4:c.2424-74_2424-71del MANE Select NP_056993.2:n.2424-74_2424-71del
NR_052013.3:n.2454-74_2454-71del