Canonical Allele Identifier: CA505189588

Gene: TUBB4A

Linked Data

• MyVariant Identifiers: chr19:g.6495835G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6495824G>C , CM000681.2:g.6495824G>C	GRCh38
NC_000019.9:g.6495835G>C , CM000681.1:g.6495835G>C	GRCh37
NC_000019.8:g.6446835G>C	NCBI36
NG_033896.1:g.12025C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264071.7:c.675C>G MANE Select	ENSP00000264071.1:p.Leu225=
ENST00000264071.6:c.675C>G	ENSP00000264071.1:p.Leu225=
ENST00000540257.5:c.675C>G	ENSP00000443590.1:p.Leu225=
ENST00000594075.5:c.465C>G	ENSP00000469936.1:p.Leu155=
ENST00000594276.5:c.363C>G	ENSP00000472481.1:p.Leu121=
ENST00000600216.5:c.417C>G	ENSP00000470983.1:p.Leu139=
NM_001289123.1:c.828C>G	NP_001276052.1:p.Leu276=
NM_001289127.1:c.810C>G	NP_001276056.1:p.Leu270=
NM_001289129.1:c.675C>G	NP_001276058.1:p.Leu225=
NM_001289130.1:c.459C>G	NP_001276059.1:p.Leu153=
NM_001289131.1:c.459C>G	NP_001276060.1:p.Leu153=
NM_006087.3:c.675C>G	NP_006078.2:p.Leu225=
NM_006087.4:c.675C>G MANE Select	NP_006078.2:p.Leu225=
NM_001289123.2:c.828C>G	NP_001276052.1:p.Leu276=
NM_001289127.2:c.810C>G	NP_001276056.1:p.Leu270=
NM_001289129.2:c.675C>G	NP_001276058.1:p.Leu225=
NM_001289130.2:c.459C>G	NP_001276059.1:p.Leu153=
NM_001289131.2:c.459C>G	NP_001276060.1:p.Leu153=