Canonical Allele Identifier: CA379562706

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111659C>A (hg19) ; chr11:g.8090112C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090112C>A , CM000673.2:g.8090112C>A	GRCh38
NC_000011.9:g.8111659C>A , CM000673.1:g.8111659C>A	GRCh37
NC_000011.8:g.8068235C>A	NCBI36
NG_029912.1:g.56480C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.134C>A MANE Select	ENSP00000299506.3:p.Pro45His
ENST00000299506.2:c.134C>A	ENSP00000299506.2:p.Pro45His
ENST00000305253.8:c.299C>A	ENSP00000305426.4:p.Pro100His
ENST00000534099.5:c.152C>A	ENSP00000434400.1:p.Pro51His
NM_003320.4:c.299C>A	NP_003311.2:p.Pro100His
NM_177972.2:c.134C>A	NP_813977.1:p.Pro45His
XM_005253109.2:c.260C>A	XP_005253166.1:p.Pro87His
XM_011520344.1:c.170C>A	XP_011518646.1:p.Pro57His
XM_005253109.3:c.260C>A	XP_005253166.1:p.Pro87His
XM_011520344.2:c.170C>A	XP_011518646.1:p.Pro57His
NM_177972.3:c.134C>A MANE Select	NP_813977.1:p.Pro45His
NM_003320.5:c.299C>A	NP_003311.2:p.Pro100His