Canonical Allele Identifier: CA379562686

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111654G>T (hg19) ; chr11:g.8090107G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090107G>T , CM000673.2:g.8090107G>T	GRCh38
NC_000011.9:g.8111654G>T , CM000673.1:g.8111654G>T	GRCh37
NC_000011.8:g.8068230G>T	NCBI36
NG_029912.1:g.56475G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.129G>T MANE Select	ENSP00000299506.3:p.Gln43His
ENST00000299506.2:c.129G>T	ENSP00000299506.2:p.Gln43His
ENST00000305253.8:c.294G>T	ENSP00000305426.4:p.Gln98His
ENST00000534099.5:c.147G>T	ENSP00000434400.1:p.Gln49His
NM_003320.4:c.294G>T	NP_003311.2:p.Gln98His
NM_177972.2:c.129G>T	NP_813977.1:p.Gln43His
XM_005253109.2:c.255G>T	XP_005253166.1:p.Gln85His
XM_011520344.1:c.165G>T	XP_011518646.1:p.Gln55His
XM_005253109.3:c.255G>T	XP_005253166.1:p.Gln85His
XM_011520344.2:c.165G>T	XP_011518646.1:p.Gln55His
NM_177972.3:c.129G>T MANE Select	NP_813977.1:p.Gln43His
NM_003320.5:c.294G>T	NP_003311.2:p.Gln98His