Canonical Allele Identifier: CA403591505
Gene: TUBB4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6495811A>T , CM000681.2:g.6495811A>T GRCh38
NC_000019.9:g.6495822A>T , CM000681.1:g.6495822A>T GRCh37
NC_000019.8:g.6446822A>T NCBI36
NG_033896.1:g.12038T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264071.7:c.688T>A MANE Select ENSP00000264071.1:p.Ser230Thr
ENST00000264071.6:c.688T>A ENSP00000264071.1:p.Ser230Thr
ENST00000540257.5:c.688T>A ENSP00000443590.1:p.Ser230Thr
ENST00000594075.5:c.478T>A ENSP00000469936.1:p.Ser160Thr
ENST00000594276.5:c.376T>A ENSP00000472481.1:p.Ser126Thr
ENST00000600216.5:c.430T>A ENSP00000470983.1:p.Ser144Thr
NM_001289123.1:c.841T>A NP_001276052.1:p.Ser281Thr
NM_001289127.1:c.823T>A NP_001276056.1:p.Ser275Thr
NM_001289129.1:c.688T>A NP_001276058.1:p.Ser230Thr
NM_001289130.1:c.472T>A NP_001276059.1:p.Ser158Thr
NM_001289131.1:c.472T>A NP_001276060.1:p.Ser158Thr
NM_006087.3:c.688T>A NP_006078.2:p.Ser230Thr
NM_006087.4:c.688T>A MANE Select NP_006078.2:p.Ser230Thr
NM_001289123.2:c.841T>A NP_001276052.1:p.Ser281Thr
NM_001289127.2:c.823T>A NP_001276056.1:p.Ser275Thr
NM_001289129.2:c.688T>A NP_001276058.1:p.Ser230Thr
NM_001289130.2:c.472T>A NP_001276059.1:p.Ser158Thr
NM_001289131.2:c.472T>A NP_001276060.1:p.Ser158Thr