Canonical Allele Identifier: CA403591603

Gene: TUBB4A

Linked Data

• COSMIC: COSM4082587
• MyVariant Identifiers: chr19:g.6495840C>A (hg19) ; chr19:g.6495829C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6495829C>A , CM000681.2:g.6495829C>A	GRCh38
NC_000019.9:g.6495840C>A , CM000681.1:g.6495840C>A	GRCh37
NC_000019.8:g.6446840C>A	NCBI36
NG_033896.1:g.12020G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264071.7:c.670G>T MANE Select	ENSP00000264071.1:p.Asp224Tyr
ENST00000264071.6:c.670G>T	ENSP00000264071.1:p.Asp224Tyr
ENST00000540257.5:c.670G>T	ENSP00000443590.1:p.Asp224Tyr
ENST00000594075.5:c.460G>T	ENSP00000469936.1:p.Asp154Tyr
ENST00000594276.5:c.358G>T	ENSP00000472481.1:p.Asp120Tyr
ENST00000600216.5:c.412G>T	ENSP00000470983.1:p.Asp138Tyr
NM_001289123.1:c.823G>T	NP_001276052.1:p.Asp275Tyr
NM_001289127.1:c.805G>T	NP_001276056.1:p.Asp269Tyr
NM_001289129.1:c.670G>T	NP_001276058.1:p.Asp224Tyr
NM_001289130.1:c.454G>T	NP_001276059.1:p.Asp152Tyr
NM_001289131.1:c.454G>T	NP_001276060.1:p.Asp152Tyr
NM_006087.3:c.670G>T	NP_006078.2:p.Asp224Tyr
NM_006087.4:c.670G>T MANE Select	NP_006078.2:p.Asp224Tyr
NM_001289123.2:c.823G>T	NP_001276052.1:p.Asp275Tyr
NM_001289127.2:c.805G>T	NP_001276056.1:p.Asp269Tyr
NM_001289129.2:c.670G>T	NP_001276058.1:p.Asp224Tyr
NM_001289130.2:c.454G>T	NP_001276059.1:p.Asp152Tyr
NM_001289131.2:c.454G>T	NP_001276060.1:p.Asp152Tyr