Canonical Allele Identifier: CA449776508

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691583T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723806T>G , CM000668.2:g.30723806T>G	GRCh38
NC_000006.11:g.30691583T>G , CM000668.1:g.30691583T>G	GRCh37
NC_000006.10:g.30799562T>G	NCBI36
NG_034142.1:g.8606T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.744T>G MANE Select	ENSP00000339001.7:p.Ala248=
ENST00000680530.1:n.1606T>G
ENST00000681421.1:n.1810T>G
ENST00000681435.1:c.528T>G	ENSP00000506665.1:p.Ala176=
ENST00000327892.12:c.744T>G	ENSP00000339001.7:p.Ala248=
ENST00000330914.7:c.528T>G	ENSP00000365578.2:p.Ala176=
ENST00000396384.1:c.528T>G	ENSP00000379668.1:p.Ala176=
ENST00000396389.5:c.690T>G	ENSP00000379672.1:p.Ala230=
NM_001293212.1:c.804T>G	NP_001280141.1:p.Ala268=
NM_001293213.1:c.370-232T>G	NP_001280142.1:n.370-232T>G
NM_001293214.1:c.612T>G	NP_001280143.1:p.Ala204=
NM_001293215.1:c.528T>G	NP_001280144.1:p.Ala176=
NM_001293216.1:c.528T>G	NP_001280145.1:p.Ala176=
NM_178014.3:c.744T>G	NP_821133.1:p.Ala248=
NR_120608.1:n.584-133T>G
NM_178014.4:c.744T>G MANE Select	NP_821133.1:p.Ala248=
NM_001293212.2:c.804T>G	NP_001280141.1:p.Ala268=
NM_001293213.2:c.370-232T>G	NP_001280142.1:n.370-232T>G
NM_001293214.2:c.612T>G	NP_001280143.1:p.Ala204=
NM_001293215.2:c.528T>G	NP_001280144.1:p.Ala176=
NM_001293216.2:c.528T>G	NP_001280145.1:p.Ala176=
NR_120608.2:n.433-133T>G