Canonical Allele Identifier: CA2612330321

Gene: TUB

Linked Data

• gnomAD v4: 11-8089511-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089511G>C , CM000673.2:g.8089511G>C	GRCh38
NC_000011.9:g.8111058G>C , CM000673.1:g.8111058G>C	GRCh37
NC_000011.8:g.8067634G>C	NCBI36
NG_029912.1:g.55879G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-99G>C MANE Select	ENSP00000299506.3:n.39-99G>C
ENST00000299506.2:c.39-99G>C	ENSP00000299506.2:n.39-99G>C
ENST00000305253.8:c.204-99G>C	ENSP00000305426.4:n.204-99G>C
ENST00000534099.5:c.57-99G>C	ENSP00000434400.1:n.57-99G>C
NM_003320.4:c.204-99G>C	NP_003311.2:n.204-99G>C
NM_177972.2:c.39-99G>C	NP_813977.1:n.39-99G>C
XM_005253109.2:c.165-99G>C	XP_005253166.1:n.165-99G>C
XM_011520344.1:c.75-99G>C	XP_011518646.1:n.75-99G>C
XM_005253109.3:c.165-99G>C	XP_005253166.1:n.165-99G>C
XM_011520344.2:c.75-99G>C	XP_011518646.1:n.75-99G>C
NM_177972.3:c.39-99G>C MANE Select	NP_813977.1:n.39-99G>C
NM_003320.5:c.204-99G>C	NP_003311.2:n.204-99G>C