Canonical Allele Identifier: CA379562916

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111712C>T (hg19) ; chr11:g.8090165C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090165C>T , CM000673.2:g.8090165C>T	GRCh38
NC_000011.9:g.8111712C>T , CM000673.1:g.8111712C>T	GRCh37
NC_000011.8:g.8068288C>T	NCBI36
NG_029912.1:g.56533C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.187C>T MANE Select	ENSP00000299506.3:p.Gln63Ter
ENST00000299506.2:c.187C>T	ENSP00000299506.2:p.Gln63Ter
ENST00000305253.8:c.352C>T	ENSP00000305426.4:p.Gln118Ter
ENST00000534099.5:c.205C>T	ENSP00000434400.1:p.Gln69Ter
NM_003320.4:c.352C>T	NP_003311.2:p.Gln118Ter
NM_177972.2:c.187C>T	NP_813977.1:p.Gln63Ter
XM_005253109.2:c.313C>T	XP_005253166.1:p.Gln105Ter
XM_011520344.1:c.223C>T	XP_011518646.1:p.Gln75Ter
XM_005253109.3:c.313C>T	XP_005253166.1:p.Gln105Ter
XM_011520344.2:c.223C>T	XP_011518646.1:p.Gln75Ter
NM_177972.3:c.187C>T MANE Select	NP_813977.1:p.Gln63Ter
NM_003320.5:c.352C>T	NP_003311.2:p.Gln118Ter