Canonical Allele Identifier: CA2490889181
Gene: NBAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15424073_15424076delinsTACC , CM000664.2:g.15424073_15424076delinsTACC GRCh38
NC_000002.11:g.15564197_15564200delinsTACC , CM000664.1:g.15564197_15564200delinsTACC GRCh37
NC_000002.10:g.15481648_15481651delinsTACC NCBI36
NG_032964.1:g.142273_142276delinsGGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.674+239_674+242delinsGGTA
ENST00000700062.1:c.674+239_674+242delinsGGTA
ENST00000700065.1:n.2590+239_2590+242delinsGGTA
ENST00000700066.1:c.2094+239_2094+242delinsGGTA ENSP00000514780.1:n.2094+239_2094+242delinsGGTA
ENST00000281513.10:c.2577+239_2577+242delinsGGTA MANE Select ENSP00000281513.5:n.2577+239_2577+242delinsGGTA
ENST00000281513.9:c.2577+239_2577+242delinsGGTA ENSP00000281513.5:n.2577+239_2577+242delinsGGTA
ENST00000441755.5:c.78+239_78+242delinsGGTA ENSP00000396501.1:n.78+239_78+242delinsGGTA
ENST00000442506.5:c.80+239_80+242delinsGGTA
NM_015909.3:c.2577+239_2577+242delinsGGTA NP_056993.2:n.2577+239_2577+242delinsGGTA
NR_052013.2:n.2621+239_2621+242delinsGGTA
XM_011510357.1:c.2448+239_2448+242delinsGGTA XP_011508659.1:n.2448+239_2448+242delinsGGTA
XM_011510358.1:c.2577+239_2577+242delinsGGTA XP_011508660.1:n.2577+239_2577+242delinsGGTA
XM_011510359.1:c.1938+239_1938+242delinsGGTA XP_011508661.1:n.1938+239_1938+242delinsGGTA
XM_011510360.1:c.378+239_378+242delinsGGTA XP_011508662.1:n.378+239_378+242delinsGGTA
XM_011510361.1:c.369+239_369+242delinsGGTA XP_011508663.1:n.369+239_369+242delinsGGTA
XM_011510357.2:c.2448+239_2448+242delinsGGTA XP_011508659.1:n.2448+239_2448+242delinsGGTA
XM_011510358.2:c.2577+239_2577+242delinsGGTA XP_011508660.1:n.2577+239_2577+242delinsGGTA
XM_011510360.2:c.378+239_378+242delinsGGTA XP_011508662.1:n.378+239_378+242delinsGGTA
XM_011510361.2:c.369+239_369+242delinsGGTA XP_011508663.1:n.369+239_369+242delinsGGTA
XM_017004317.1:c.2577+239_2577+242delinsGGTA XP_016859806.1:n.2577+239_2577+242delinsGGTA
XM_024452961.1:c.1938+239_1938+242delinsGGTA XP_024308729.1:n.1938+239_1938+242delinsGGTA
NM_015909.4:c.2577+239_2577+242delinsGGTA MANE Select NP_056993.2:n.2577+239_2577+242delinsGGTA
NR_052013.3:n.2607+239_2607+242delinsGGTA