Canonical Allele Identifier: CA2320458755

Gene: TUBB4A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6495818G= , CM000681.2:g.6495818G=	GRCh38
NC_000019.9:g.6495829G= , CM000681.1:g.6495829G=	GRCh37
NC_000019.8:g.6446829G=	NCBI36
NG_033896.1:g.12031C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264071.7:c.681C= MANE Select	ENSP00000264071.1:p.His227=
ENST00000264071.6:c.681C=	ENSP00000264071.1:p.His227=
ENST00000540257.5:c.681C=	ENSP00000443590.1:p.His227=
ENST00000594075.5:c.471C=	ENSP00000469936.1:p.His157=
ENST00000594276.5:c.369C=	ENSP00000472481.1:p.His123=
ENST00000600216.5:c.423C=	ENSP00000470983.1:p.His141=
NM_001289123.1:c.834C=	NP_001276052.1:p.His278=
NM_001289127.1:c.816C=	NP_001276056.1:p.His272=
NM_001289129.1:c.681C=	NP_001276058.1:p.His227=
NM_001289130.1:c.465C=	NP_001276059.1:p.His155=
NM_001289131.1:c.465C=	NP_001276060.1:p.His155=
NM_006087.3:c.681C=	NP_006078.2:p.His227=
NM_006087.4:c.681C= MANE Select	NP_006078.2:p.His227=
NM_001289123.2:c.834C=	NP_001276052.1:p.His278=
NM_001289127.2:c.816C=	NP_001276056.1:p.His272=
NM_001289129.2:c.681C=	NP_001276058.1:p.His227=
NM_001289130.2:c.465C=	NP_001276059.1:p.His155=
NM_001289131.2:c.465C=	NP_001276060.1:p.His155=