Canonical Allele Identifier: CA2612330595

Gene: TUB

Linked Data

• gnomAD v4: 11-8090256-T-TCCCGTCACTGCTTCGGGGAG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090266_8090285dup , CM000673.2:g.8090266_8090285dup	GRCh38
NC_000011.9:g.8111813_8111832dup , CM000673.1:g.8111813_8111832dup	GRCh37
NC_000011.8:g.8068389_8068408dup	NCBI36
NG_029912.1:g.56634_56653dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.253+35_253+54dup MANE Select	ENSP00000299506.3:n.253+35_253+54dup
ENST00000299506.2:c.253+35_253+54dup	ENSP00000299506.2:n.253+35_253+54dup
ENST00000305253.8:c.418+35_418+54dup	ENSP00000305426.4:n.418+35_418+54dup
ENST00000534099.5:c.271+35_271+54dup	ENSP00000434400.1:n.271+35_271+54dup
NM_003320.4:c.418+35_418+54dup	NP_003311.2:n.418+35_418+54dup
NM_177972.2:c.253+35_253+54dup	NP_813977.1:n.253+35_253+54dup
XM_005253109.2:c.379+35_379+54dup	XP_005253166.1:n.379+35_379+54dup
XM_011520344.1:c.289+35_289+54dup	XP_011518646.1:n.289+35_289+54dup
XM_005253109.3:c.379+35_379+54dup	XP_005253166.1:n.379+35_379+54dup
XM_011520344.2:c.289+35_289+54dup	XP_011518646.1:n.289+35_289+54dup
NM_177972.3:c.253+35_253+54dup MANE Select	NP_813977.1:n.253+35_253+54dup
NM_003320.5:c.418+35_418+54dup	NP_003311.2:n.418+35_418+54dup