Canonical Allele Identifier: CA1618847610

Gene: TUBB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724025G= , CM000668.2:g.30724025G=	GRCh38
NC_000006.11:g.30691802G= , CM000668.1:g.30691802G=	GRCh37
NC_000006.10:g.30799781G=	NCBI36
NG_034142.1:g.8825G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.963G= MANE Select	ENSP00000339001.7:p.Met321=
ENST00000680530.1:n.1825G=
ENST00000681421.1:n.2029G=
ENST00000681435.1:c.747G=	ENSP00000506665.1:p.Met249=
ENST00000327892.12:c.963G=	ENSP00000339001.7:p.Met321=
ENST00000330914.7:c.747G=	ENSP00000365578.2:p.Met249=
ENST00000396384.1:c.747G=	ENSP00000379668.1:p.Met249=
ENST00000396389.5:c.909G=	ENSP00000379672.1:p.Met303=
NM_001293212.1:c.1023G=	NP_001280141.1:p.Met341=
NM_001293213.1:c.370-13G=	NP_001280142.1:n.370-13G=
NM_001293214.1:c.831G=	NP_001280143.1:p.Met277=
NM_001293215.1:c.747G=	NP_001280144.1:p.Met249=
NM_001293216.1:c.747G=	NP_001280145.1:p.Met249=
NM_178014.3:c.963G=	NP_821133.1:p.Met321=
NR_120608.1:n.670G=
NM_178014.4:c.963G= MANE Select	NP_821133.1:p.Met321=
NM_001293212.2:c.1023G=	NP_001280141.1:p.Met341=
NM_001293213.2:c.370-13G=	NP_001280142.1:n.370-13G=
NM_001293214.2:c.831G=	NP_001280143.1:p.Met277=
NM_001293215.2:c.747G=	NP_001280144.1:p.Met249=
NM_001293216.2:c.747G=	NP_001280145.1:p.Met249=
NR_120608.2:n.519G=