Canonical Allele Identifier: CA345890107
Gene: NBAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15424425A>T , CM000664.2:g.15424425A>T GRCh38
NC_000002.11:g.15564549A>T , CM000664.1:g.15564549A>T GRCh37
NC_000002.10:g.15482000A>T NCBI36
NG_032964.1:g.141924T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.564T>A
ENST00000700062.1:c.564T>A
ENST00000700065.1:n.2480T>A
ENST00000700066.1:c.1984T>A ENSP00000514780.1:p.Tyr662Asn
ENST00000281513.10:c.2467T>A MANE Select ENSP00000281513.5:p.Tyr823Asn
ENST00000281513.9:c.2467T>A ENSP00000281513.5:p.Tyr823Asn
NM_015909.3:c.2467T>A NP_056993.2:p.Tyr823Asn
NR_052013.2:n.2511T>A
XM_011510357.1:c.2338T>A XP_011508659.1:p.Tyr780Asn
XM_011510358.1:c.2467T>A XP_011508660.1:p.Tyr823Asn
XM_011510359.1:c.1828T>A XP_011508661.1:p.Tyr610Asn
XM_011510360.1:c.268T>A XP_011508662.1:p.Tyr90Asn
XM_011510361.1:c.259T>A XP_011508663.1:p.Tyr87Asn
XM_011510357.2:c.2338T>A XP_011508659.1:p.Tyr780Asn
XM_011510358.2:c.2467T>A XP_011508660.1:p.Tyr823Asn
XM_011510360.2:c.268T>A XP_011508662.1:p.Tyr90Asn
XM_011510361.2:c.259T>A XP_011508663.1:p.Tyr87Asn
XM_017004317.1:c.2467T>A XP_016859806.1:p.Tyr823Asn
XM_024452961.1:c.1828T>A XP_024308729.1:p.Tyr610Asn
NM_015909.4:c.2467T>A MANE Select NP_056993.2:p.Tyr823Asn
NR_052013.3:n.2497T>A