Canonical Allele Identifier: CA363149049

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691732A>G (hg19) ; chr6:g.30723955A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723955A>G , CM000668.2:g.30723955A>G	GRCh38
NC_000006.11:g.30691732A>G , CM000668.1:g.30691732A>G	GRCh37
NC_000006.10:g.30799711A>G	NCBI36
NG_034142.1:g.8755A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.893A>G MANE Select	ENSP00000339001.7:p.Asn298Ser
ENST00000680530.1:n.1755A>G
ENST00000681421.1:n.1959A>G
ENST00000681435.1:c.677A>G	ENSP00000506665.1:p.Asn226Ser
ENST00000327892.12:c.893A>G	ENSP00000339001.7:p.Asn298Ser
ENST00000330914.7:c.677A>G	ENSP00000365578.2:p.Asn226Ser
ENST00000396384.1:c.677A>G	ENSP00000379668.1:p.Asn226Ser
ENST00000396389.5:c.839A>G	ENSP00000379672.1:p.Asn280Ser
NM_001293212.1:c.953A>G	NP_001280141.1:p.Asn318Ser
NM_001293213.1:c.370-83A>G	NP_001280142.1:n.370-83A>G
NM_001293214.1:c.761A>G	NP_001280143.1:p.Asn254Ser
NM_001293215.1:c.677A>G	NP_001280144.1:p.Asn226Ser
NM_001293216.1:c.677A>G	NP_001280145.1:p.Asn226Ser
NM_178014.3:c.893A>G	NP_821133.1:p.Asn298Ser
NR_120608.1:n.600A>G
NM_178014.4:c.893A>G MANE Select	NP_821133.1:p.Asn298Ser
NM_001293212.2:c.953A>G	NP_001280141.1:p.Asn318Ser
NM_001293213.2:c.370-83A>G	NP_001280142.1:n.370-83A>G
NM_001293214.2:c.761A>G	NP_001280143.1:p.Asn254Ser
NM_001293215.2:c.677A>G	NP_001280144.1:p.Asn226Ser
NM_001293216.2:c.677A>G	NP_001280145.1:p.Asn226Ser
NR_120608.2:n.449A>G