Canonical Allele Identifier: CA363149269

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691762G>A (hg19) ; chr6:g.30723985G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723985G>A , CM000668.2:g.30723985G>A	GRCh38
NC_000006.11:g.30691762G>A , CM000668.1:g.30691762G>A	GRCh37
NC_000006.10:g.30799741G>A	NCBI36
NG_034142.1:g.8785G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.923G>A MANE Select	ENSP00000339001.7:p.Gly308Asp
ENST00000680530.1:n.1785G>A
ENST00000681421.1:n.1989G>A
ENST00000681435.1:c.707G>A	ENSP00000506665.1:p.Gly236Asp
ENST00000327892.12:c.923G>A	ENSP00000339001.7:p.Gly308Asp
ENST00000330914.7:c.707G>A	ENSP00000365578.2:p.Gly236Asp
ENST00000396384.1:c.707G>A	ENSP00000379668.1:p.Gly236Asp
ENST00000396389.5:c.869G>A	ENSP00000379672.1:p.Gly290Asp
NM_001293212.1:c.983G>A	NP_001280141.1:p.Gly328Asp
NM_001293213.1:c.370-53G>A	NP_001280142.1:n.370-53G>A
NM_001293214.1:c.791G>A	NP_001280143.1:p.Gly264Asp
NM_001293215.1:c.707G>A	NP_001280144.1:p.Gly236Asp
NM_001293216.1:c.707G>A	NP_001280145.1:p.Gly236Asp
NM_178014.3:c.923G>A	NP_821133.1:p.Gly308Asp
NR_120608.1:n.630G>A
NM_178014.4:c.923G>A MANE Select	NP_821133.1:p.Gly308Asp
NM_001293212.2:c.983G>A	NP_001280141.1:p.Gly328Asp
NM_001293213.2:c.370-53G>A	NP_001280142.1:n.370-53G>A
NM_001293214.2:c.791G>A	NP_001280143.1:p.Gly264Asp
NM_001293215.2:c.707G>A	NP_001280144.1:p.Gly236Asp
NM_001293216.2:c.707G>A	NP_001280145.1:p.Gly236Asp
NR_120608.2:n.479G>A