Canonical Allele Identifier: CA2790351919

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090247T>A , CM000673.2:g.8090247T>A	GRCh38
NC_000011.9:g.8111794T>A , CM000673.1:g.8111794T>A	GRCh37
NC_000011.8:g.8068370T>A	NCBI36
NG_029912.1:g.56615T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.253+16T>A MANE Select	ENSP00000299506.3:n.253+16T>A
ENST00000299506.2:c.253+16T>A	ENSP00000299506.2:n.253+16T>A
ENST00000305253.8:c.418+16T>A	ENSP00000305426.4:n.418+16T>A
ENST00000534099.5:c.271+16T>A	ENSP00000434400.1:n.271+16T>A
NM_003320.4:c.418+16T>A	NP_003311.2:n.418+16T>A
NM_177972.2:c.253+16T>A	NP_813977.1:n.253+16T>A
XM_005253109.2:c.379+16T>A	XP_005253166.1:n.379+16T>A
XM_011520344.1:c.289+16T>A	XP_011518646.1:n.289+16T>A
XM_005253109.3:c.379+16T>A	XP_005253166.1:n.379+16T>A
XM_011520344.2:c.289+16T>A	XP_011518646.1:n.289+16T>A
NM_177972.3:c.253+16T>A MANE Select	NP_813977.1:n.253+16T>A
NM_003320.5:c.418+16T>A	NP_003311.2:n.418+16T>A