Canonical Allele Identifier: CA1536041
Gene: NBAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15379868G>T , CM000664.2:g.15379868G>T GRCh38
NC_000002.11:g.15519992G>T , CM000664.1:g.15519992G>T GRCh37
NC_000002.10:g.15437443G>T NCBI36
NG_032964.1:g.186481C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.1458-37C>A
ENST00000700062.1:c.1458-37C>A
ENST00000700065.1:n.3374-37C>A
ENST00000281513.10:c.3361-37C>A MANE Select ENSP00000281513.5:n.3361-37C>A
ENST00000281513.9:c.3361-37C>A ENSP00000281513.5:n.3361-37C>A
ENST00000441755.5:c.502-37C>A ENSP00000396501.1:n.502-37C>A
ENST00000442506.5:c.504-37C>A
NM_015909.3:c.3361-37C>A NP_056993.2:n.3361-37C>A
NR_052013.2:n.3405-37C>A
XM_011510357.1:c.3232-37C>A XP_011508659.1:n.3232-37C>A
XM_011510358.1:c.3361-37C>A XP_011508660.1:n.3361-37C>A
XM_011510359.1:c.2722-37C>A XP_011508661.1:n.2722-37C>A
XM_011510360.1:c.1162-37C>A XP_011508662.1:n.1162-37C>A
XM_011510361.1:c.1153-37C>A XP_011508663.1:n.1153-37C>A
XM_011510357.2:c.3232-37C>A XP_011508659.1:n.3232-37C>A
XM_011510358.2:c.3361-37C>A XP_011508660.1:n.3361-37C>A
XM_011510360.2:c.1162-37C>A XP_011508662.1:n.1162-37C>A
XM_011510361.2:c.1153-37C>A XP_011508663.1:n.1153-37C>A
XM_017004317.1:c.3361-37C>A XP_016859806.1:n.3361-37C>A
XM_024452961.1:c.2722-37C>A XP_024308729.1:n.2722-37C>A
NM_015909.4:c.3361-37C>A MANE Select NP_056993.2:n.3361-37C>A
NR_052013.3:n.3391-37C>A