Canonical Allele Identifier: CA403591440
Gene: TUBB4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6495798C>G , CM000681.2:g.6495798C>G GRCh38
NC_000019.9:g.6495809C>G , CM000681.1:g.6495809C>G GRCh37
NC_000019.8:g.6446809C>G NCBI36
NG_033896.1:g.12051G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264071.7:c.701G>C MANE Select ENSP00000264071.1:p.Ser234Thr
ENST00000264071.6:c.701G>C ENSP00000264071.1:p.Ser234Thr
ENST00000540257.5:c.701G>C ENSP00000443590.1:p.Ser234Thr
ENST00000594276.5:c.389G>C ENSP00000472481.1:p.Ser130Thr
NM_001289123.1:c.854G>C NP_001276052.1:p.Ser285Thr
NM_001289127.1:c.836G>C NP_001276056.1:p.Ser279Thr
NM_001289129.1:c.701G>C NP_001276058.1:p.Ser234Thr
NM_001289130.1:c.485G>C NP_001276059.1:p.Ser162Thr
NM_001289131.1:c.485G>C NP_001276060.1:p.Ser162Thr
NM_006087.3:c.701G>C NP_006078.2:p.Ser234Thr
NM_006087.4:c.701G>C MANE Select NP_006078.2:p.Ser234Thr
NM_001289123.2:c.854G>C NP_001276052.1:p.Ser285Thr
NM_001289127.2:c.836G>C NP_001276056.1:p.Ser279Thr
NM_001289129.2:c.701G>C NP_001276058.1:p.Ser234Thr
NM_001289130.2:c.485G>C NP_001276059.1:p.Ser162Thr
NM_001289131.2:c.485G>C NP_001276060.1:p.Ser162Thr