Canonical Allele Identifier: CA403591191

Gene: TUBB4A

Linked Data

• MyVariant Identifiers: chr19:g.6495764T>C (hg19) ; chr19:g.6495753T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6495753T>C , CM000681.2:g.6495753T>C	GRCh38
NC_000019.9:g.6495764T>C , CM000681.1:g.6495764T>C	GRCh37
NC_000019.8:g.6446764T>C	NCBI36
NG_033896.1:g.12096A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264071.7:c.746A>G MANE Select	ENSP00000264071.1:p.Asp249Gly
ENST00000264071.6:c.746A>G	ENSP00000264071.1:p.Asp249Gly
ENST00000540257.5:c.746A>G	ENSP00000443590.1:p.Asp249Gly
ENST00000594276.5:c.434A>G	ENSP00000472481.1:p.Asp145Gly
NM_001289123.1:c.899A>G	NP_001276052.1:p.Asp300Gly
NM_001289127.1:c.881A>G	NP_001276056.1:p.Asp294Gly
NM_001289129.1:c.746A>G	NP_001276058.1:p.Asp249Gly
NM_001289130.1:c.530A>G	NP_001276059.1:p.Asp177Gly
NM_001289131.1:c.530A>G	NP_001276060.1:p.Asp177Gly
NM_006087.3:c.746A>G	NP_006078.2:p.Asp249Gly
NM_006087.4:c.746A>G MANE Select	NP_006078.2:p.Asp249Gly
NM_001289123.2:c.899A>G	NP_001276052.1:p.Asp300Gly
NM_001289127.2:c.881A>G	NP_001276056.1:p.Asp294Gly
NM_001289129.2:c.746A>G	NP_001276058.1:p.Asp249Gly
NM_001289130.2:c.530A>G	NP_001276059.1:p.Asp177Gly
NM_001289131.2:c.530A>G	NP_001276060.1:p.Asp177Gly