Canonical Allele Identifier: CA2320458740

Gene: TUBB4A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6495793C= , CM000681.2:g.6495793C=	GRCh38
NC_000019.9:g.6495804C= , CM000681.1:g.6495804C=	GRCh37
NC_000019.8:g.6446804C=	NCBI36
NG_033896.1:g.12056G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264071.7:c.706G= MANE Select	ENSP00000264071.1:p.Val236=
ENST00000264071.6:c.706G=	ENSP00000264071.1:p.Val236=
ENST00000540257.5:c.706G=	ENSP00000443590.1:p.Val236=
ENST00000594276.5:c.394G=	ENSP00000472481.1:p.Val132=
NM_001289123.1:c.859G=	NP_001276052.1:p.Val287=
NM_001289127.1:c.841G=	NP_001276056.1:p.Val281=
NM_001289129.1:c.706G=	NP_001276058.1:p.Val236=
NM_001289130.1:c.490G=	NP_001276059.1:p.Val164=
NM_001289131.1:c.490G=	NP_001276060.1:p.Val164=
NM_006087.3:c.706G=	NP_006078.2:p.Val236=
NM_006087.4:c.706G= MANE Select	NP_006078.2:p.Val236=
NM_001289123.2:c.859G=	NP_001276052.1:p.Val287=
NM_001289127.2:c.841G=	NP_001276056.1:p.Val281=
NM_001289129.2:c.706G=	NP_001276058.1:p.Val236=
NM_001289130.2:c.490G=	NP_001276059.1:p.Val164=
NM_001289131.2:c.490G=	NP_001276060.1:p.Val164=