Canonical Allele Identifier: CA363151269

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30692002T>G (hg19) ; chr6:g.30724225T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724225T>G , CM000668.2:g.30724225T>G	GRCh38
NC_000006.11:g.30692002T>G , CM000668.1:g.30692002T>G	GRCh37
NC_000006.10:g.30799981T>G	NCBI36
NG_034142.1:g.9025T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1163T>G MANE Select	ENSP00000339001.7:p.Met388Arg
ENST00000680530.1:n.2025T>G
ENST00000681421.1:n.2229T>G
ENST00000681435.1:c.947T>G	ENSP00000506665.1:p.Met316Arg
ENST00000327892.12:c.1163T>G	ENSP00000339001.7:p.Met388Arg
ENST00000330914.7:c.947T>G	ENSP00000365578.2:p.Met316Arg
ENST00000396384.1:c.947T>G	ENSP00000379668.1:p.Met316Arg
ENST00000396389.5:c.1109T>G	ENSP00000379672.1:p.Met370Arg
NM_001293212.1:c.1223T>G	NP_001280141.1:p.Met408Arg
NM_001293213.1:c.557T>G	NP_001280142.1:p.Met186Arg
NM_001293214.1:c.1031T>G	NP_001280143.1:p.Met344Arg
NM_001293215.1:c.947T>G	NP_001280144.1:p.Met316Arg
NM_001293216.1:c.947T>G	NP_001280145.1:p.Met316Arg
NM_178014.3:c.1163T>G	NP_821133.1:p.Met388Arg
NR_120608.1:n.870T>G
NM_178014.4:c.1163T>G MANE Select	NP_821133.1:p.Met388Arg
NM_001293212.2:c.1223T>G	NP_001280141.1:p.Met408Arg
NM_001293213.2:c.557T>G	NP_001280142.1:p.Met186Arg
NM_001293214.2:c.1031T>G	NP_001280143.1:p.Met344Arg
NM_001293215.2:c.947T>G	NP_001280144.1:p.Met316Arg
NM_001293216.2:c.947T>G	NP_001280145.1:p.Met316Arg
NR_120608.2:n.719T>G