Canonical Allele Identifier: CA403591158

Gene: TUBB4A

Linked Data

• MyVariant Identifiers: chr19:g.6495758C>G (hg19) ; chr19:g.6495747C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6495747C>G , CM000681.2:g.6495747C>G	GRCh38
NC_000019.9:g.6495758C>G , CM000681.1:g.6495758C>G	GRCh37
NC_000019.8:g.6446758C>G	NCBI36
NG_033896.1:g.12102G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264071.7:c.752G>C MANE Select	ENSP00000264071.1:p.Arg251Pro
ENST00000264071.6:c.752G>C	ENSP00000264071.1:p.Arg251Pro
ENST00000540257.5:c.752G>C	ENSP00000443590.1:p.Arg251Pro
ENST00000594276.5:c.440G>C	ENSP00000472481.1:p.Arg147Pro
NM_001289123.1:c.905G>C	NP_001276052.1:p.Arg302Pro
NM_001289127.1:c.887G>C	NP_001276056.1:p.Arg296Pro
NM_001289129.1:c.752G>C	NP_001276058.1:p.Arg251Pro
NM_001289130.1:c.536G>C	NP_001276059.1:p.Arg179Pro
NM_001289131.1:c.536G>C	NP_001276060.1:p.Arg179Pro
NM_006087.3:c.752G>C	NP_006078.2:p.Arg251Pro
NM_006087.4:c.752G>C MANE Select	NP_006078.2:p.Arg251Pro
NM_001289123.2:c.905G>C	NP_001276052.1:p.Arg302Pro
NM_001289127.2:c.887G>C	NP_001276056.1:p.Arg296Pro
NM_001289129.2:c.752G>C	NP_001276058.1:p.Arg251Pro
NM_001289130.2:c.536G>C	NP_001276059.1:p.Arg179Pro
NM_001289131.2:c.536G>C	NP_001276060.1:p.Arg179Pro