Canonical Allele Identifier: CA2657930779
Gene: NBAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15219093_15219094insG , CM000664.2:g.15219093_15219094insG GRCh38
NC_000002.11:g.15359217_15359218insG , CM000664.1:g.15359217_15359218insG GRCh37
NC_000002.10:g.15276668_15276669insG NCBI36
NG_032964.1:g.347255_347256insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.4223-126_4223-125insC
ENST00000700062.1:c.4426+13328_4426+13329insC
ENST00000700063.1:c.748-126_748-125insC
ENST00000700064.1:c.2093-126_2093-125insC
ENST00000281513.10:c.6237-126_6237-125insC MANE Select ENSP00000281513.5:n.6237-126_6237-125insC
ENST00000281513.9:c.6237-126_6237-125insC ENSP00000281513.5:n.6237-126_6237-125insC
ENST00000417461.5:c.512+13328_512+13329insC ENSP00000392421.1:n.512+13328_512+13329insC
ENST00000442506.5:c.3380-126_3380-125insC
NM_015909.3:c.6237-126_6237-125insC NP_056993.2:n.6237-126_6237-125insC
NR_052013.2:n.6280+13328_6280+13329insC
XM_011510357.1:c.6108-126_6108-125insC XP_011508659.1:n.6108-126_6108-125insC
XM_011510358.1:c.6237-126_6237-125insC XP_011508660.1:n.6237-126_6237-125insC
XM_011510359.1:c.5598-126_5598-125insC XP_011508661.1:n.5598-126_5598-125insC
XM_011510360.1:c.4038-126_4038-125insC XP_011508662.1:n.4038-126_4038-125insC
XM_011510361.1:c.4029-126_4029-125insC XP_011508663.1:n.4029-126_4029-125insC
XM_011510357.2:c.6108-126_6108-125insC XP_011508659.1:n.6108-126_6108-125insC
XM_011510358.2:c.6237-126_6237-125insC XP_011508660.1:n.6237-126_6237-125insC
XM_011510360.2:c.4038-126_4038-125insC XP_011508662.1:n.4038-126_4038-125insC
XM_011510361.2:c.4029-126_4029-125insC XP_011508663.1:n.4029-126_4029-125insC
XM_017004317.1:c.6237-126_6237-125insC XP_016859806.1:n.6237-126_6237-125insC
XM_024452961.1:c.5598-126_5598-125insC XP_024308729.1:n.5598-126_5598-125insC
NM_015909.4:c.6237-126_6237-125insC MANE Select NP_056993.2:n.6237-126_6237-125insC
NR_052013.3:n.6266+13328_6266+13329insC