Canonical Allele Identifier: CA2790352733

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089393_8089394dup , CM000673.2:g.8089393_8089394dup	GRCh38
NC_000011.9:g.8110940_8110941dup , CM000673.1:g.8110940_8110941dup	GRCh37
NC_000011.8:g.8067516_8067517dup	NCBI36
NG_029912.1:g.55761_55762dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-217_39-216dup MANE Select	ENSP00000299506.3:n.39-217_39-216dup
ENST00000299506.2:c.39-217_39-216dup	ENSP00000299506.2:n.39-217_39-216dup
ENST00000305253.8:c.204-217_204-216dup	ENSP00000305426.4:n.204-217_204-216dup
ENST00000534099.5:c.57-217_57-216dup	ENSP00000434400.1:n.57-217_57-216dup
NM_003320.4:c.204-217_204-216dup	NP_003311.2:n.204-217_204-216dup
NM_177972.2:c.39-217_39-216dup	NP_813977.1:n.39-217_39-216dup
XM_005253109.2:c.165-217_165-216dup	XP_005253166.1:n.165-217_165-216dup
XM_011520344.1:c.75-217_75-216dup	XP_011518646.1:n.75-217_75-216dup
XM_005253109.3:c.165-217_165-216dup	XP_005253166.1:n.165-217_165-216dup
XM_011520344.2:c.75-217_75-216dup	XP_011518646.1:n.75-217_75-216dup
NM_177972.3:c.39-217_39-216dup MANE Select	NP_813977.1:n.39-217_39-216dup
NM_003320.5:c.204-217_204-216dup	NP_003311.2:n.204-217_204-216dup