Canonical Allele Identifier: CA345889838
Gene: NBAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15424386G>T , CM000664.2:g.15424386G>T GRCh38
NC_000002.11:g.15564510G>T , CM000664.1:g.15564510G>T GRCh37
NC_000002.10:g.15481961G>T NCBI36
NG_032964.1:g.141963C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.603C>A
ENST00000700062.1:c.603C>A
ENST00000700065.1:n.2519C>A
ENST00000700066.1:c.2023C>A ENSP00000514780.1:p.Gln675Lys
ENST00000281513.10:c.2506C>A MANE Select ENSP00000281513.5:p.Gln836Lys
ENST00000281513.9:c.2506C>A ENSP00000281513.5:p.Gln836Lys
ENST00000441755.5:c.7C>A ENSP00000396501.1:p.Gln3Lys
ENST00000442506.5:c.9C>A
NM_015909.3:c.2506C>A NP_056993.2:p.Gln836Lys
NR_052013.2:n.2550C>A
XM_011510357.1:c.2377C>A XP_011508659.1:p.Gln793Lys
XM_011510358.1:c.2506C>A XP_011508660.1:p.Gln836Lys
XM_011510359.1:c.1867C>A XP_011508661.1:p.Gln623Lys
XM_011510360.1:c.307C>A XP_011508662.1:p.Gln103Lys
XM_011510361.1:c.298C>A XP_011508663.1:p.Gln100Lys
XM_011510357.2:c.2377C>A XP_011508659.1:p.Gln793Lys
XM_011510358.2:c.2506C>A XP_011508660.1:p.Gln836Lys
XM_011510360.2:c.307C>A XP_011508662.1:p.Gln103Lys
XM_011510361.2:c.298C>A XP_011508663.1:p.Gln100Lys
XM_017004317.1:c.2506C>A XP_016859806.1:p.Gln836Lys
XM_024452961.1:c.1867C>A XP_024308729.1:p.Gln623Lys
NM_015909.4:c.2506C>A MANE Select NP_056993.2:p.Gln836Lys
NR_052013.3:n.2536C>A