Canonical Allele Identifier: CA379562742

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111667G>A (hg19) ; chr11:g.8090120G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090120G>A , CM000673.2:g.8090120G>A	GRCh38
NC_000011.9:g.8111667G>A , CM000673.1:g.8111667G>A	GRCh37
NC_000011.8:g.8068243G>A	NCBI36
NG_029912.1:g.56488G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.142G>A MANE Select	ENSP00000299506.3:p.Val48Met
ENST00000299506.2:c.142G>A	ENSP00000299506.2:p.Val48Met
ENST00000305253.8:c.307G>A	ENSP00000305426.4:p.Val103Met
ENST00000534099.5:c.160G>A	ENSP00000434400.1:p.Val54Met
NM_003320.4:c.307G>A	NP_003311.2:p.Val103Met
NM_177972.2:c.142G>A	NP_813977.1:p.Val48Met
XM_005253109.2:c.268G>A	XP_005253166.1:p.Val90Met
XM_011520344.1:c.178G>A	XP_011518646.1:p.Val60Met
XM_005253109.3:c.268G>A	XP_005253166.1:p.Val90Met
XM_011520344.2:c.178G>A	XP_011518646.1:p.Val60Met
NM_177972.3:c.142G>A MANE Select	NP_813977.1:p.Val48Met
NM_003320.5:c.307G>A	NP_003311.2:p.Val103Met