Canonical Allele Identifier: CA449776620

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691628C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723851C>A , CM000668.2:g.30723851C>A	GRCh38
NC_000006.11:g.30691628C>A , CM000668.1:g.30691628C>A	GRCh37
NC_000006.10:g.30799607C>A	NCBI36
NG_034142.1:g.8651C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.789C>A MANE Select	ENSP00000339001.7:p.Leu263=
ENST00000680530.1:n.1651C>A
ENST00000681421.1:n.1855C>A
ENST00000681435.1:c.573C>A	ENSP00000506665.1:p.Leu191=
ENST00000327892.12:c.789C>A	ENSP00000339001.7:p.Leu263=
ENST00000330914.7:c.573C>A	ENSP00000365578.2:p.Leu191=
ENST00000396384.1:c.573C>A	ENSP00000379668.1:p.Leu191=
ENST00000396389.5:c.735C>A	ENSP00000379672.1:p.Leu245=
NM_001293212.1:c.849C>A	NP_001280141.1:p.Leu283=
NM_001293213.1:c.370-187C>A	NP_001280142.1:n.370-187C>A
NM_001293214.1:c.657C>A	NP_001280143.1:p.Leu219=
NM_001293215.1:c.573C>A	NP_001280144.1:p.Leu191=
NM_001293216.1:c.573C>A	NP_001280145.1:p.Leu191=
NM_178014.3:c.789C>A	NP_821133.1:p.Leu263=
NR_120608.1:n.584-88C>A
NM_178014.4:c.789C>A MANE Select	NP_821133.1:p.Leu263=
NM_001293212.2:c.849C>A	NP_001280141.1:p.Leu283=
NM_001293213.2:c.370-187C>A	NP_001280142.1:n.370-187C>A
NM_001293214.2:c.657C>A	NP_001280143.1:p.Leu219=
NM_001293215.2:c.573C>A	NP_001280144.1:p.Leu191=
NM_001293216.2:c.573C>A	NP_001280145.1:p.Leu191=
NR_120608.2:n.433-88C>A