Canonical Allele Identifier: CA449776551

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691598G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723821G>A , CM000668.2:g.30723821G>A	GRCh38
NC_000006.11:g.30691598G>A , CM000668.1:g.30691598G>A	GRCh37
NC_000006.10:g.30799577G>A	NCBI36
NG_034142.1:g.8621G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.759G>A MANE Select	ENSP00000339001.7:p.Leu253=
ENST00000680530.1:n.1621G>A
ENST00000681421.1:n.1825G>A
ENST00000681435.1:c.543G>A	ENSP00000506665.1:p.Leu181=
ENST00000327892.12:c.759G>A	ENSP00000339001.7:p.Leu253=
ENST00000330914.7:c.543G>A	ENSP00000365578.2:p.Leu181=
ENST00000396384.1:c.543G>A	ENSP00000379668.1:p.Leu181=
ENST00000396389.5:c.705G>A	ENSP00000379672.1:p.Leu235=
NM_001293212.1:c.819G>A	NP_001280141.1:p.Leu273=
NM_001293213.1:c.370-217G>A	NP_001280142.1:n.370-217G>A
NM_001293214.1:c.627G>A	NP_001280143.1:p.Leu209=
NM_001293215.1:c.543G>A	NP_001280144.1:p.Leu181=
NM_001293216.1:c.543G>A	NP_001280145.1:p.Leu181=
NM_178014.3:c.759G>A	NP_821133.1:p.Leu253=
NR_120608.1:n.584-118G>A
NM_178014.4:c.759G>A MANE Select	NP_821133.1:p.Leu253=
NM_001293212.2:c.819G>A	NP_001280141.1:p.Leu273=
NM_001293213.2:c.370-217G>A	NP_001280142.1:n.370-217G>A
NM_001293214.2:c.627G>A	NP_001280143.1:p.Leu209=
NM_001293215.2:c.543G>A	NP_001280144.1:p.Leu181=
NM_001293216.2:c.543G>A	NP_001280145.1:p.Leu181=
NR_120608.2:n.433-118G>A