Canonical Allele Identifier: CA345881990
Gene: NBAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15402214A>T , CM000664.2:g.15402214A>T GRCh38
NC_000002.11:g.15542338A>T , CM000664.1:g.15542338A>T GRCh37
NC_000002.10:g.15459789A>T NCBI36
NG_032964.1:g.164135T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.1122T>A
ENST00000700062.1:c.1122T>A
ENST00000700065.1:n.3038T>A
ENST00000281513.10:c.3025T>A MANE Select ENSP00000281513.5:p.Cys1009Ser
ENST00000281513.9:c.3025T>A ENSP00000281513.5:p.Cys1009Ser
ENST00000429842.1:c.317T>A
ENST00000441755.5:c.166T>A ENSP00000396501.1:p.Cys56Ser
ENST00000442506.5:c.168T>A
NM_015909.3:c.3025T>A NP_056993.2:p.Cys1009Ser
NR_052013.2:n.3069T>A
XM_011510357.1:c.2896T>A XP_011508659.1:p.Cys966Ser
XM_011510358.1:c.3025T>A XP_011508660.1:p.Cys1009Ser
XM_011510359.1:c.2386T>A XP_011508661.1:p.Cys796Ser
XM_011510360.1:c.826T>A XP_011508662.1:p.Cys276Ser
XM_011510361.1:c.817T>A XP_011508663.1:p.Cys273Ser
XM_011510357.2:c.2896T>A XP_011508659.1:p.Cys966Ser
XM_011510358.2:c.3025T>A XP_011508660.1:p.Cys1009Ser
XM_011510360.2:c.826T>A XP_011508662.1:p.Cys276Ser
XM_011510361.2:c.817T>A XP_011508663.1:p.Cys273Ser
XM_017004317.1:c.3025T>A XP_016859806.1:p.Cys1009Ser
XM_024452961.1:c.2386T>A XP_024308729.1:p.Cys796Ser
NM_015909.4:c.3025T>A MANE Select NP_056993.2:p.Cys1009Ser
NR_052013.3:n.3055T>A