Canonical Allele Identifier: CA1618847586

Gene: TUBB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723889G= , CM000668.2:g.30723889G=	GRCh38
NC_000006.11:g.30691666G= , CM000668.1:g.30691666G=	GRCh37
NC_000006.10:g.30799645G=	NCBI36
NG_034142.1:g.8689G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.827G= MANE Select	ENSP00000339001.7:p.Arg276=
ENST00000680530.1:n.1689G=
ENST00000681421.1:n.1893G=
ENST00000681435.1:c.611G=	ENSP00000506665.1:p.Arg204=
ENST00000327892.12:c.827G=	ENSP00000339001.7:p.Arg276=
ENST00000330914.7:c.611G=	ENSP00000365578.2:p.Arg204=
ENST00000396384.1:c.611G=	ENSP00000379668.1:p.Arg204=
ENST00000396389.5:c.773G=	ENSP00000379672.1:p.Arg258=
NM_001293212.1:c.887G=	NP_001280141.1:p.Arg296=
NM_001293213.1:c.370-149G=	NP_001280142.1:n.370-149G=
NM_001293214.1:c.695G=	NP_001280143.1:p.Arg232=
NM_001293215.1:c.611G=	NP_001280144.1:p.Arg204=
NM_001293216.1:c.611G=	NP_001280145.1:p.Arg204=
NM_178014.3:c.827G=	NP_821133.1:p.Arg276=
NR_120608.1:n.584-50G=
NM_178014.4:c.827G= MANE Select	NP_821133.1:p.Arg276=
NM_001293212.2:c.887G=	NP_001280141.1:p.Arg296=
NM_001293213.2:c.370-149G=	NP_001280142.1:n.370-149G=
NM_001293214.2:c.695G=	NP_001280143.1:p.Arg232=
NM_001293215.2:c.611G=	NP_001280144.1:p.Arg204=
NM_001293216.2:c.611G=	NP_001280145.1:p.Arg204=
NR_120608.2:n.433-50G=