Canonical Allele Identifier: CA2320458726

Gene: TUBB4A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6495787T= , CM000681.2:g.6495787T=	GRCh38
NC_000019.9:g.6495798T= , CM000681.1:g.6495798T=	GRCh37
NC_000019.8:g.6446798T=	NCBI36
NG_033896.1:g.12062A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264071.7:c.712A= MANE Select	ENSP00000264071.1:p.Thr238=
ENST00000264071.6:c.712A=	ENSP00000264071.1:p.Thr238=
ENST00000540257.5:c.712A=	ENSP00000443590.1:p.Thr238=
ENST00000594276.5:c.400A=	ENSP00000472481.1:p.Thr134=
NM_001289123.1:c.865A=	NP_001276052.1:p.Thr289=
NM_001289127.1:c.847A=	NP_001276056.1:p.Thr283=
NM_001289129.1:c.712A=	NP_001276058.1:p.Thr238=
NM_001289130.1:c.496A=	NP_001276059.1:p.Thr166=
NM_001289131.1:c.496A=	NP_001276060.1:p.Thr166=
NM_006087.3:c.712A=	NP_006078.2:p.Thr238=
NM_006087.4:c.712A= MANE Select	NP_006078.2:p.Thr238=
NM_001289123.2:c.865A=	NP_001276052.1:p.Thr289=
NM_001289127.2:c.847A=	NP_001276056.1:p.Thr283=
NM_001289129.2:c.712A=	NP_001276058.1:p.Thr238=
NM_001289130.2:c.496A=	NP_001276059.1:p.Thr166=
NM_001289131.2:c.496A=	NP_001276060.1:p.Thr166=