Canonical Allele Identifier: CA379562522

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111614A>C (hg19) ; chr11:g.8090067A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090067A>C , CM000673.2:g.8090067A>C	GRCh38
NC_000011.9:g.8111614A>C , CM000673.1:g.8111614A>C	GRCh37
NC_000011.8:g.8068190A>C	NCBI36
NG_029912.1:g.56435A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.91-2A>C MANE Select	ENSP00000299506.3:n.91-2A>C
ENST00000299506.2:c.91-2A>C	ENSP00000299506.2:n.91-2A>C
ENST00000305253.8:c.256-2A>C	ENSP00000305426.4:n.256-2A>C
ENST00000534099.5:c.109-2A>C	ENSP00000434400.1:n.109-2A>C
NM_003320.4:c.256-2A>C	NP_003311.2:n.256-2A>C
NM_177972.2:c.91-2A>C	NP_813977.1:n.91-2A>C
XM_005253109.2:c.217-2A>C	XP_005253166.1:n.217-2A>C
XM_011520344.1:c.127-2A>C	XP_011518646.1:n.127-2A>C
XM_005253109.3:c.217-2A>C	XP_005253166.1:n.217-2A>C
XM_011520344.2:c.127-2A>C	XP_011518646.1:n.127-2A>C
NM_177972.3:c.91-2A>C MANE Select	NP_813977.1:n.91-2A>C
NM_003320.5:c.256-2A>C	NP_003311.2:n.256-2A>C