Canonical Allele Identifier: CA217415090

Gene: TUB

Linked Data

• dbSNP Id: rs938944019
• MyVariant Identifiers: chr11:g.8111186G>T (hg19) ; chr11:g.8089639G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089639G>T , CM000673.2:g.8089639G>T	GRCh38
NC_000011.9:g.8111186G>T , CM000673.1:g.8111186G>T	GRCh37
NC_000011.8:g.8067762G>T	NCBI36
NG_029912.1:g.56007G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.68G>T MANE Select	ENSP00000299506.3:p.Arg23Met
ENST00000299506.2:c.68G>T	ENSP00000299506.2:p.Arg23Met
ENST00000305253.8:c.233G>T	ENSP00000305426.4:p.Arg78Met
ENST00000534099.5:c.86G>T	ENSP00000434400.1:p.Arg29Met
NM_003320.4:c.233G>T	NP_003311.2:p.Arg78Met
NM_177972.2:c.68G>T	NP_813977.1:p.Arg23Met
XM_005253109.2:c.194G>T	XP_005253166.1:p.Arg65Met
XM_011520344.1:c.104G>T	XP_011518646.1:p.Arg35Met
XM_005253109.3:c.194G>T	XP_005253166.1:p.Arg65Met
XM_011520344.2:c.104G>T	XP_011518646.1:p.Arg35Met
NM_177972.3:c.68G>T MANE Select	NP_813977.1:p.Arg23Met
NM_003320.5:c.233G>T	NP_003311.2:p.Arg78Met