Canonical Allele Identifier: CA1618847604

Gene: TUBB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723983C= , CM000668.2:g.30723983C=	GRCh38
NC_000006.11:g.30691760C= , CM000668.1:g.30691760C=	GRCh37
NC_000006.10:g.30799739C=	NCBI36
NG_034142.1:g.8783C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.921C= MANE Select	ENSP00000339001.7:p.His307=
ENST00000680530.1:n.1783C=
ENST00000681421.1:n.1987C=
ENST00000681435.1:c.705C=	ENSP00000506665.1:p.His235=
ENST00000327892.12:c.921C=	ENSP00000339001.7:p.His307=
ENST00000330914.7:c.705C=	ENSP00000365578.2:p.His235=
ENST00000396384.1:c.705C=	ENSP00000379668.1:p.His235=
ENST00000396389.5:c.867C=	ENSP00000379672.1:p.His289=
NM_001293212.1:c.981C=	NP_001280141.1:p.His327=
NM_001293213.1:c.370-55C=	NP_001280142.1:n.370-55C=
NM_001293214.1:c.789C=	NP_001280143.1:p.His263=
NM_001293215.1:c.705C=	NP_001280144.1:p.His235=
NM_001293216.1:c.705C=	NP_001280145.1:p.His235=
NM_178014.3:c.921C=	NP_821133.1:p.His307=
NR_120608.1:n.628C=
NM_178014.4:c.921C= MANE Select	NP_821133.1:p.His307=
NM_001293212.2:c.981C=	NP_001280141.1:p.His327=
NM_001293213.2:c.370-55C=	NP_001280142.1:n.370-55C=
NM_001293214.2:c.789C=	NP_001280143.1:p.His263=
NM_001293215.2:c.705C=	NP_001280144.1:p.His235=
NM_001293216.2:c.705C=	NP_001280145.1:p.His235=
NR_120608.2:n.477C=