Canonical Allele Identifier: CA403591453

Gene: TUBB4A

Linked Data

• MyVariant Identifiers: chr19:g.6495812A>C (hg19) ; chr19:g.6495801A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6495801A>C , CM000681.2:g.6495801A>C	GRCh38
NC_000019.9:g.6495812A>C , CM000681.1:g.6495812A>C	GRCh37
NC_000019.8:g.6446812A>C	NCBI36
NG_033896.1:g.12048T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264071.7:c.698T>G MANE Select	ENSP00000264071.1:p.Met233Arg
ENST00000264071.6:c.698T>G	ENSP00000264071.1:p.Met233Arg
ENST00000540257.5:c.698T>G	ENSP00000443590.1:p.Met233Arg
ENST00000594276.5:c.386T>G	ENSP00000472481.1:p.Met129Arg
NM_001289123.1:c.851T>G	NP_001276052.1:p.Met284Arg
NM_001289127.1:c.833T>G	NP_001276056.1:p.Met278Arg
NM_001289129.1:c.698T>G	NP_001276058.1:p.Met233Arg
NM_001289130.1:c.482T>G	NP_001276059.1:p.Met161Arg
NM_001289131.1:c.482T>G	NP_001276060.1:p.Met161Arg
NM_006087.3:c.698T>G	NP_006078.2:p.Met233Arg
NM_006087.4:c.698T>G MANE Select	NP_006078.2:p.Met233Arg
NM_001289123.2:c.851T>G	NP_001276052.1:p.Met284Arg
NM_001289127.2:c.833T>G	NP_001276056.1:p.Met278Arg
NM_001289129.2:c.698T>G	NP_001276058.1:p.Met233Arg
NM_001289130.2:c.482T>G	NP_001276059.1:p.Met161Arg
NM_001289131.2:c.482T>G	NP_001276060.1:p.Met161Arg