Canonical Allele Identifier: CA363148495

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691605A>T (hg19) ; chr6:g.30723828A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723828A>T , CM000668.2:g.30723828A>T	GRCh38
NC_000006.11:g.30691605A>T , CM000668.1:g.30691605A>T	GRCh37
NC_000006.10:g.30799584A>T	NCBI36
NG_034142.1:g.8628A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.766A>T MANE Select	ENSP00000339001.7:p.Asn256Tyr
ENST00000680530.1:n.1628A>T
ENST00000681421.1:n.1832A>T
ENST00000681435.1:c.550A>T	ENSP00000506665.1:p.Asn184Tyr
ENST00000327892.12:c.766A>T	ENSP00000339001.7:p.Asn256Tyr
ENST00000330914.7:c.550A>T	ENSP00000365578.2:p.Asn184Tyr
ENST00000396384.1:c.550A>T	ENSP00000379668.1:p.Asn184Tyr
ENST00000396389.5:c.712A>T	ENSP00000379672.1:p.Asn238Tyr
NM_001293212.1:c.826A>T	NP_001280141.1:p.Asn276Tyr
NM_001293213.1:c.370-210A>T	NP_001280142.1:n.370-210A>T
NM_001293214.1:c.634A>T	NP_001280143.1:p.Asn212Tyr
NM_001293215.1:c.550A>T	NP_001280144.1:p.Asn184Tyr
NM_001293216.1:c.550A>T	NP_001280145.1:p.Asn184Tyr
NM_178014.3:c.766A>T	NP_821133.1:p.Asn256Tyr
NR_120608.1:n.584-111A>T
NM_178014.4:c.766A>T MANE Select	NP_821133.1:p.Asn256Tyr
NM_001293212.2:c.826A>T	NP_001280141.1:p.Asn276Tyr
NM_001293213.2:c.370-210A>T	NP_001280142.1:n.370-210A>T
NM_001293214.2:c.634A>T	NP_001280143.1:p.Asn212Tyr
NM_001293215.2:c.550A>T	NP_001280144.1:p.Asn184Tyr
NM_001293216.2:c.550A>T	NP_001280145.1:p.Asn184Tyr
NR_120608.2:n.433-111A>T