Canonical Allele Identifier: CA363148377

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691582C>G (hg19) ; chr6:g.30723805C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723805C>G , CM000668.2:g.30723805C>G	GRCh38
NC_000006.11:g.30691582C>G , CM000668.1:g.30691582C>G	GRCh37
NC_000006.10:g.30799561C>G	NCBI36
NG_034142.1:g.8605C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.743C>G MANE Select	ENSP00000339001.7:p.Ala248Gly
ENST00000680530.1:n.1605C>G
ENST00000681421.1:n.1809C>G
ENST00000681435.1:c.527C>G	ENSP00000506665.1:p.Ala176Gly
ENST00000327892.12:c.743C>G	ENSP00000339001.7:p.Ala248Gly
ENST00000330914.7:c.527C>G	ENSP00000365578.2:p.Ala176Gly
ENST00000396384.1:c.527C>G	ENSP00000379668.1:p.Ala176Gly
ENST00000396389.5:c.689C>G	ENSP00000379672.1:p.Ala230Gly
NM_001293212.1:c.803C>G	NP_001280141.1:p.Ala268Gly
NM_001293213.1:c.370-233C>G	NP_001280142.1:n.370-233C>G
NM_001293214.1:c.611C>G	NP_001280143.1:p.Ala204Gly
NM_001293215.1:c.527C>G	NP_001280144.1:p.Ala176Gly
NM_001293216.1:c.527C>G	NP_001280145.1:p.Ala176Gly
NM_178014.3:c.743C>G	NP_821133.1:p.Ala248Gly
NR_120608.1:n.584-134C>G
NM_178014.4:c.743C>G MANE Select	NP_821133.1:p.Ala248Gly
NM_001293212.2:c.803C>G	NP_001280141.1:p.Ala268Gly
NM_001293213.2:c.370-233C>G	NP_001280142.1:n.370-233C>G
NM_001293214.2:c.611C>G	NP_001280143.1:p.Ala204Gly
NM_001293215.2:c.527C>G	NP_001280144.1:p.Ala176Gly
NM_001293216.2:c.527C>G	NP_001280145.1:p.Ala176Gly
NR_120608.2:n.433-134C>G