Canonical Allele Identifier: CA1618847581

Gene: TUBB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723875C= , CM000668.2:g.30723875C=	GRCh38
NC_000006.11:g.30691652C= , CM000668.1:g.30691652C=	GRCh37
NC_000006.10:g.30799631C=	NCBI36
NG_034142.1:g.8675C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.813C= MANE Select	ENSP00000339001.7:p.Ala271=
ENST00000680530.1:n.1675C=
ENST00000681421.1:n.1879C=
ENST00000681435.1:c.597C=	ENSP00000506665.1:p.Ala199=
ENST00000327892.12:c.813C=	ENSP00000339001.7:p.Ala271=
ENST00000330914.7:c.597C=	ENSP00000365578.2:p.Ala199=
ENST00000396384.1:c.597C=	ENSP00000379668.1:p.Ala199=
ENST00000396389.5:c.759C=	ENSP00000379672.1:p.Ala253=
NM_001293212.1:c.873C=	NP_001280141.1:p.Ala291=
NM_001293213.1:c.370-163C=	NP_001280142.1:n.370-163C=
NM_001293214.1:c.681C=	NP_001280143.1:p.Ala227=
NM_001293215.1:c.597C=	NP_001280144.1:p.Ala199=
NM_001293216.1:c.597C=	NP_001280145.1:p.Ala199=
NM_178014.3:c.813C=	NP_821133.1:p.Ala271=
NR_120608.1:n.584-64C=
NM_178014.4:c.813C= MANE Select	NP_821133.1:p.Ala271=
NM_001293212.2:c.873C=	NP_001280141.1:p.Ala291=
NM_001293213.2:c.370-163C=	NP_001280142.1:n.370-163C=
NM_001293214.2:c.681C=	NP_001280143.1:p.Ala227=
NM_001293215.2:c.597C=	NP_001280144.1:p.Ala199=
NM_001293216.2:c.597C=	NP_001280145.1:p.Ala199=
NR_120608.2:n.433-64C=