Canonical Allele Identifier: CA1618847657

Gene: TUBB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724268C= , CM000668.2:g.30724268C=	GRCh38
NC_000006.11:g.30692045C= , CM000668.1:g.30692045C=	GRCh37
NC_000006.10:g.30800024C=	NCBI36
NG_034142.1:g.9068C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1206C= MANE Select	ENSP00000339001.7:p.Gly402=
ENST00000680530.1:n.2068C=
ENST00000681421.1:n.2272C=
ENST00000681435.1:c.990C=	ENSP00000506665.1:p.Gly330=
ENST00000327892.12:c.1206C=	ENSP00000339001.7:p.Gly402=
ENST00000330914.7:c.990C=	ENSP00000365578.2:p.Gly330=
ENST00000396384.1:c.990C=	ENSP00000379668.1:p.Gly330=
ENST00000396389.5:c.1152C=	ENSP00000379672.1:p.Gly384=
NM_001293212.1:c.1266C=	NP_001280141.1:p.Gly422=
NM_001293213.1:c.600C=	NP_001280142.1:p.Gly200=
NM_001293214.1:c.1074C=	NP_001280143.1:p.Gly358=
NM_001293215.1:c.990C=	NP_001280144.1:p.Gly330=
NM_001293216.1:c.990C=	NP_001280145.1:p.Gly330=
NM_178014.3:c.1206C=	NP_821133.1:p.Gly402=
NR_120608.1:n.913C=
NM_178014.4:c.1206C= MANE Select	NP_821133.1:p.Gly402=
NM_001293212.2:c.1266C=	NP_001280141.1:p.Gly422=
NM_001293213.2:c.600C=	NP_001280142.1:p.Gly200=
NM_001293214.2:c.1074C=	NP_001280143.1:p.Gly358=
NM_001293215.2:c.990C=	NP_001280144.1:p.Gly330=
NM_001293216.2:c.990C=	NP_001280145.1:p.Gly330=
NR_120608.2:n.762C=