Canonical Allele Identifier: CA345884738
Gene: NBAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15218897A>C , CM000664.2:g.15218897A>C GRCh38
NC_000002.11:g.15359021A>C , CM000664.1:g.15359021A>C GRCh37
NC_000002.10:g.15276472A>C NCBI36
NG_032964.1:g.347452T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.4294T>G
ENST00000700062.1:c.4426+13525T>G
ENST00000700063.1:c.819T>G
ENST00000700064.1:c.2164T>G
ENST00000281513.10:c.6308T>G MANE Select ENSP00000281513.5:p.Val2103Gly
ENST00000281513.9:c.6308T>G ENSP00000281513.5:p.Val2103Gly
ENST00000417461.5:c.512+13525T>G ENSP00000392421.1:n.512+13525T>G
ENST00000442506.5:c.3451T>G
NM_015909.3:c.6308T>G NP_056993.2:p.Val2103Gly
NR_052013.2:n.6280+13525T>G
XM_011510357.1:c.6179T>G XP_011508659.1:p.Val2060Gly
XM_011510358.1:c.6308T>G XP_011508660.1:p.Val2103Gly
XM_011510359.1:c.5669T>G XP_011508661.1:p.Val1890Gly
XM_011510360.1:c.4109T>G XP_011508662.1:p.Val1370Gly
XM_011510361.1:c.4100T>G XP_011508663.1:p.Val1367Gly
XM_011510357.2:c.6179T>G XP_011508659.1:p.Val2060Gly
XM_011510358.2:c.6308T>G XP_011508660.1:p.Val2103Gly
XM_011510360.2:c.4109T>G XP_011508662.1:p.Val1370Gly
XM_011510361.2:c.4100T>G XP_011508663.1:p.Val1367Gly
XM_017004317.1:c.6308T>G XP_016859806.1:p.Val2103Gly
XM_024452961.1:c.5669T>G XP_024308729.1:p.Val1890Gly
NM_015909.4:c.6308T>G MANE Select NP_056993.2:p.Val2103Gly
NR_052013.3:n.6266+13525T>G