Canonical Allele Identifier: CA363150881

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691952C>A (hg19) ; chr6:g.30724175C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724175C>A , CM000668.2:g.30724175C>A	GRCh38
NC_000006.11:g.30691952C>A , CM000668.1:g.30691952C>A	GRCh37
NC_000006.10:g.30799931C>A	NCBI36
NG_034142.1:g.8975C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1113C>A MANE Select	ENSP00000339001.7:p.Ser371Arg
ENST00000680530.1:n.1975C>A
ENST00000681421.1:n.2179C>A
ENST00000681435.1:c.897C>A	ENSP00000506665.1:p.Ser299Arg
ENST00000327892.12:c.1113C>A	ENSP00000339001.7:p.Ser371Arg
ENST00000330914.7:c.897C>A	ENSP00000365578.2:p.Ser299Arg
ENST00000396384.1:c.897C>A	ENSP00000379668.1:p.Ser299Arg
ENST00000396389.5:c.1059C>A	ENSP00000379672.1:p.Ser353Arg
NM_001293212.1:c.1173C>A	NP_001280141.1:p.Ser391Arg
NM_001293213.1:c.507C>A	NP_001280142.1:p.Ser169Arg
NM_001293214.1:c.981C>A	NP_001280143.1:p.Ser327Arg
NM_001293215.1:c.897C>A	NP_001280144.1:p.Ser299Arg
NM_001293216.1:c.897C>A	NP_001280145.1:p.Ser299Arg
NM_178014.3:c.1113C>A	NP_821133.1:p.Ser371Arg
NR_120608.1:n.820C>A
NM_178014.4:c.1113C>A MANE Select	NP_821133.1:p.Ser371Arg
NM_001293212.2:c.1173C>A	NP_001280141.1:p.Ser391Arg
NM_001293213.2:c.507C>A	NP_001280142.1:p.Ser169Arg
NM_001293214.2:c.981C>A	NP_001280143.1:p.Ser327Arg
NM_001293215.2:c.897C>A	NP_001280144.1:p.Ser299Arg
NM_001293216.2:c.897C>A	NP_001280145.1:p.Ser299Arg
NR_120608.2:n.669C>A