Canonical Allele Identifier: CA217415721

Gene: TUB

Linked Data

• dbSNP Id: rs1039068749
• MyVariant Identifiers: chr11:g.8111778G>C (hg19) ; chr11:g.8090231G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090231G>C , CM000673.2:g.8090231G>C	GRCh38
NC_000011.9:g.8111778G>C , CM000673.1:g.8111778G>C	GRCh37
NC_000011.8:g.8068354G>C	NCBI36
NG_029912.1:g.56599G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.253G>C MANE Select	ENSP00000299506.3:p.Val85Leu
ENST00000299506.2:c.253G>C	ENSP00000299506.2:p.Val85Leu
ENST00000305253.8:c.418G>C	ENSP00000305426.4:p.Val140Leu
ENST00000534099.5:c.271G>C	ENSP00000434400.1:p.Val91Leu
NM_003320.4:c.418G>C	NP_003311.2:p.Val140Leu
NM_177972.2:c.253G>C	NP_813977.1:p.Val85Leu
XM_005253109.2:c.379G>C	XP_005253166.1:p.Val127Leu
XM_011520344.1:c.289G>C	XP_011518646.1:p.Val97Leu
XM_005253109.3:c.379G>C	XP_005253166.1:p.Val127Leu
XM_011520344.2:c.289G>C	XP_011518646.1:p.Val97Leu
NM_177972.3:c.253G>C MANE Select	NP_813977.1:p.Val85Leu
NM_003320.5:c.418G>C	NP_003311.2:p.Val140Leu