Canonical Allele Identifier: CA345890103
Gene: NBAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15424424T>A , CM000664.2:g.15424424T>A GRCh38
NC_000002.11:g.15564548T>A , CM000664.1:g.15564548T>A GRCh37
NC_000002.10:g.15481999T>A NCBI36
NG_032964.1:g.141925A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000700061.1:c.565A>T
ENST00000700062.1:c.565A>T
ENST00000700065.1:n.2481A>T
ENST00000700066.1:c.1985A>T ENSP00000514780.1:p.Tyr662Phe
ENST00000281513.10:c.2468A>T MANE Select ENSP00000281513.5:p.Tyr823Phe
ENST00000281513.9:c.2468A>T ENSP00000281513.5:p.Tyr823Phe
NM_015909.3:c.2468A>T NP_056993.2:p.Tyr823Phe
NR_052013.2:n.2512A>T
XM_011510357.1:c.2339A>T XP_011508659.1:p.Tyr780Phe
XM_011510358.1:c.2468A>T XP_011508660.1:p.Tyr823Phe
XM_011510359.1:c.1829A>T XP_011508661.1:p.Tyr610Phe
XM_011510360.1:c.269A>T XP_011508662.1:p.Tyr90Phe
XM_011510361.1:c.260A>T XP_011508663.1:p.Tyr87Phe
XM_011510357.2:c.2339A>T XP_011508659.1:p.Tyr780Phe
XM_011510358.2:c.2468A>T XP_011508660.1:p.Tyr823Phe
XM_011510360.2:c.269A>T XP_011508662.1:p.Tyr90Phe
XM_011510361.2:c.260A>T XP_011508663.1:p.Tyr87Phe
XM_017004317.1:c.2468A>T XP_016859806.1:p.Tyr823Phe
XM_024452961.1:c.1829A>T XP_024308729.1:p.Tyr610Phe
NM_015909.4:c.2468A>T MANE Select NP_056993.2:p.Tyr823Phe
NR_052013.3:n.2498A>T