Canonical Allele Identifier: CA403591460
Gene: TUBB4A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.6495802T>A , CM000681.2:g.6495802T>A GRCh38
NC_000019.9:g.6495813T>A , CM000681.1:g.6495813T>A GRCh37
NC_000019.8:g.6446813T>A NCBI36
NG_033896.1:g.12047A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264071.7:c.697A>T MANE Select ENSP00000264071.1:p.Met233Leu
ENST00000264071.6:c.697A>T ENSP00000264071.1:p.Met233Leu
ENST00000540257.5:c.697A>T ENSP00000443590.1:p.Met233Leu
ENST00000594276.5:c.385A>T ENSP00000472481.1:p.Met129Leu
NM_001289123.1:c.850A>T NP_001276052.1:p.Met284Leu
NM_001289127.1:c.832A>T NP_001276056.1:p.Met278Leu
NM_001289129.1:c.697A>T NP_001276058.1:p.Met233Leu
NM_001289130.1:c.481A>T NP_001276059.1:p.Met161Leu
NM_001289131.1:c.481A>T NP_001276060.1:p.Met161Leu
NM_006087.3:c.697A>T NP_006078.2:p.Met233Leu
NM_006087.4:c.697A>T MANE Select NP_006078.2:p.Met233Leu
NM_001289123.2:c.850A>T NP_001276052.1:p.Met284Leu
NM_001289127.2:c.832A>T NP_001276056.1:p.Met278Leu
NM_001289129.2:c.697A>T NP_001276058.1:p.Met233Leu
NM_001289130.2:c.481A>T NP_001276059.1:p.Met161Leu
NM_001289131.2:c.481A>T NP_001276060.1:p.Met161Leu