Canonical Allele Identifier: CA449776771

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691712G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723935G>A , CM000668.2:g.30723935G>A	GRCh38
NC_000006.11:g.30691712G>A , CM000668.1:g.30691712G>A	GRCh37
NC_000006.10:g.30799691G>A	NCBI36
NG_034142.1:g.8735G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.873G>A MANE Select	ENSP00000339001.7:p.Gln291=
ENST00000680530.1:n.1735G>A
ENST00000681421.1:n.1939G>A
ENST00000681435.1:c.657G>A	ENSP00000506665.1:p.Gln219=
ENST00000327892.12:c.873G>A	ENSP00000339001.7:p.Gln291=
ENST00000330914.7:c.657G>A	ENSP00000365578.2:p.Gln219=
ENST00000396384.1:c.657G>A	ENSP00000379668.1:p.Gln219=
ENST00000396389.5:c.819G>A	ENSP00000379672.1:p.Gln273=
NM_001293212.1:c.933G>A	NP_001280141.1:p.Gln311=
NM_001293213.1:c.370-103G>A	NP_001280142.1:n.370-103G>A
NM_001293214.1:c.741G>A	NP_001280143.1:p.Gln247=
NM_001293215.1:c.657G>A	NP_001280144.1:p.Gln219=
NM_001293216.1:c.657G>A	NP_001280145.1:p.Gln219=
NM_178014.3:c.873G>A	NP_821133.1:p.Gln291=
NR_120608.1:n.584-4G>A
NM_178014.4:c.873G>A MANE Select	NP_821133.1:p.Gln291=
NM_001293212.2:c.933G>A	NP_001280141.1:p.Gln311=
NM_001293213.2:c.370-103G>A	NP_001280142.1:n.370-103G>A
NM_001293214.2:c.741G>A	NP_001280143.1:p.Gln247=
NM_001293215.2:c.657G>A	NP_001280144.1:p.Gln219=
NM_001293216.2:c.657G>A	NP_001280145.1:p.Gln219=
NR_120608.2:n.433-4G>A