Canonical Allele Identifier: CA2790351920

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090258_8090259insACAA , CM000673.2:g.8090258_8090259insACAA	GRCh38
NC_000011.9:g.8111805_8111806insACAA , CM000673.1:g.8111805_8111806insACAA	GRCh37
NC_000011.8:g.8068381_8068382insACAA	NCBI36
NG_029912.1:g.56626_56627insACAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.253+27_253+28insACAA MANE Select	ENSP00000299506.3:n.253+27_253+28insACAA
ENST00000299506.2:c.253+27_253+28insACAA	ENSP00000299506.2:n.253+27_253+28insACAA
ENST00000305253.8:c.418+27_418+28insACAA	ENSP00000305426.4:n.418+27_418+28insACAA
ENST00000534099.5:c.271+27_271+28insACAA	ENSP00000434400.1:n.271+27_271+28insACAA
NM_003320.4:c.418+27_418+28insACAA	NP_003311.2:n.418+27_418+28insACAA
NM_177972.2:c.253+27_253+28insACAA	NP_813977.1:n.253+27_253+28insACAA
XM_005253109.2:c.379+27_379+28insACAA	XP_005253166.1:n.379+27_379+28insACAA
XM_011520344.1:c.289+27_289+28insACAA	XP_011518646.1:n.289+27_289+28insACAA
XM_005253109.3:c.379+27_379+28insACAA	XP_005253166.1:n.379+27_379+28insACAA
XM_011520344.2:c.289+27_289+28insACAA	XP_011518646.1:n.289+27_289+28insACAA
NM_177972.3:c.253+27_253+28insACAA MANE Select	NP_813977.1:n.253+27_253+28insACAA
NM_003320.5:c.418+27_418+28insACAA	NP_003311.2:n.418+27_418+28insACAA