Canonical Allele Identifier: CA363148782

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691674C>T (hg19) ; chr6:g.30723897C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723897C>T , CM000668.2:g.30723897C>T	GRCh38
NC_000006.11:g.30691674C>T , CM000668.1:g.30691674C>T	GRCh37
NC_000006.10:g.30799653C>T	NCBI36
NG_034142.1:g.8697C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.835C>T MANE Select	ENSP00000339001.7:p.Gln279Ter
ENST00000680530.1:n.1697C>T
ENST00000681421.1:n.1901C>T
ENST00000681435.1:c.619C>T	ENSP00000506665.1:p.Gln207Ter
ENST00000327892.12:c.835C>T	ENSP00000339001.7:p.Gln279Ter
ENST00000330914.7:c.619C>T	ENSP00000365578.2:p.Gln207Ter
ENST00000396384.1:c.619C>T	ENSP00000379668.1:p.Gln207Ter
ENST00000396389.5:c.781C>T	ENSP00000379672.1:p.Gln261Ter
NM_001293212.1:c.895C>T	NP_001280141.1:p.Gln299Ter
NM_001293213.1:c.370-141C>T	NP_001280142.1:n.370-141C>T
NM_001293214.1:c.703C>T	NP_001280143.1:p.Gln235Ter
NM_001293215.1:c.619C>T	NP_001280144.1:p.Gln207Ter
NM_001293216.1:c.619C>T	NP_001280145.1:p.Gln207Ter
NM_178014.3:c.835C>T	NP_821133.1:p.Gln279Ter
NR_120608.1:n.584-42C>T
NM_178014.4:c.835C>T MANE Select	NP_821133.1:p.Gln279Ter
NM_001293212.2:c.895C>T	NP_001280141.1:p.Gln299Ter
NM_001293213.2:c.370-141C>T	NP_001280142.1:n.370-141C>T
NM_001293214.2:c.703C>T	NP_001280143.1:p.Gln235Ter
NM_001293215.2:c.619C>T	NP_001280144.1:p.Gln207Ter
NM_001293216.2:c.619C>T	NP_001280145.1:p.Gln207Ter
NR_120608.2:n.433-42C>T