Canonical Allele Identifier: CA379562751

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111668T>A (hg19) ; chr11:g.8090121T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090121T>A , CM000673.2:g.8090121T>A	GRCh38
NC_000011.9:g.8111668T>A , CM000673.1:g.8111668T>A	GRCh37
NC_000011.8:g.8068244T>A	NCBI36
NG_029912.1:g.56489T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.143T>A MANE Select	ENSP00000299506.3:p.Val48Glu
ENST00000299506.2:c.143T>A	ENSP00000299506.2:p.Val48Glu
ENST00000305253.8:c.308T>A	ENSP00000305426.4:p.Val103Glu
ENST00000534099.5:c.161T>A	ENSP00000434400.1:p.Val54Glu
NM_003320.4:c.308T>A	NP_003311.2:p.Val103Glu
NM_177972.2:c.143T>A	NP_813977.1:p.Val48Glu
XM_005253109.2:c.269T>A	XP_005253166.1:p.Val90Glu
XM_011520344.1:c.179T>A	XP_011518646.1:p.Val60Glu
XM_005253109.3:c.269T>A	XP_005253166.1:p.Val90Glu
XM_011520344.2:c.179T>A	XP_011518646.1:p.Val60Glu
NM_177972.3:c.143T>A MANE Select	NP_813977.1:p.Val48Glu
NM_003320.5:c.308T>A	NP_003311.2:p.Val103Glu