Canonical Allele Identifier: CA449776978

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691931A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724154A>T , CM000668.2:g.30724154A>T	GRCh38
NC_000006.11:g.30691931A>T , CM000668.1:g.30691931A>T	GRCh37
NC_000006.10:g.30799910A>T	NCBI36
NG_034142.1:g.8954A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1092A>T MANE Select	ENSP00000339001.7:p.Ala364=
ENST00000680530.1:n.1954A>T
ENST00000681421.1:n.2158A>T
ENST00000681435.1:c.876A>T	ENSP00000506665.1:p.Ala292=
ENST00000327892.12:c.1092A>T	ENSP00000339001.7:p.Ala364=
ENST00000330914.7:c.876A>T	ENSP00000365578.2:p.Ala292=
ENST00000396384.1:c.876A>T	ENSP00000379668.1:p.Ala292=
ENST00000396389.5:c.1038A>T	ENSP00000379672.1:p.Ala346=
NM_001293212.1:c.1152A>T	NP_001280141.1:p.Ala384=
NM_001293213.1:c.486A>T	NP_001280142.1:p.Ala162=
NM_001293214.1:c.960A>T	NP_001280143.1:p.Ala320=
NM_001293215.1:c.876A>T	NP_001280144.1:p.Ala292=
NM_001293216.1:c.876A>T	NP_001280145.1:p.Ala292=
NM_178014.3:c.1092A>T	NP_821133.1:p.Ala364=
NR_120608.1:n.799A>T
NM_178014.4:c.1092A>T MANE Select	NP_821133.1:p.Ala364=
NM_001293212.2:c.1152A>T	NP_001280141.1:p.Ala384=
NM_001293213.2:c.486A>T	NP_001280142.1:p.Ala162=
NM_001293214.2:c.960A>T	NP_001280143.1:p.Ala320=
NM_001293215.2:c.876A>T	NP_001280144.1:p.Ala292=
NM_001293216.2:c.876A>T	NP_001280145.1:p.Ala292=
NR_120608.2:n.648A>T