Canonical Allele Identifier: CA2320458760

Gene: TUBB4A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.6495822T= , CM000681.2:g.6495822T=	GRCh38
NC_000019.9:g.6495833T= , CM000681.1:g.6495833T=	GRCh37
NC_000019.8:g.6446833T=	NCBI36
NG_033896.1:g.12027A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264071.7:c.677A= MANE Select	ENSP00000264071.1:p.Asn226=
ENST00000264071.6:c.677A=	ENSP00000264071.1:p.Asn226=
ENST00000540257.5:c.677A=	ENSP00000443590.1:p.Asn226=
ENST00000594075.5:c.467A=	ENSP00000469936.1:p.Asn156=
ENST00000594276.5:c.365A=	ENSP00000472481.1:p.Asn122=
ENST00000600216.5:c.419A=	ENSP00000470983.1:p.Asn140=
NM_001289123.1:c.830A=	NP_001276052.1:p.Asn277=
NM_001289127.1:c.812A=	NP_001276056.1:p.Asn271=
NM_001289129.1:c.677A=	NP_001276058.1:p.Asn226=
NM_001289130.1:c.461A=	NP_001276059.1:p.Asn154=
NM_001289131.1:c.461A=	NP_001276060.1:p.Asn154=
NM_006087.3:c.677A=	NP_006078.2:p.Asn226=
NM_006087.4:c.677A= MANE Select	NP_006078.2:p.Asn226=
NM_001289123.2:c.830A=	NP_001276052.1:p.Asn277=
NM_001289127.2:c.812A=	NP_001276056.1:p.Asn271=
NM_001289129.2:c.677A=	NP_001276058.1:p.Asn226=
NM_001289130.2:c.461A=	NP_001276059.1:p.Asn154=
NM_001289131.2:c.461A=	NP_001276060.1:p.Asn154=