Canonical Allele Identifier: CA2790351916

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090240T>C , CM000673.2:g.8090240T>C	GRCh38
NC_000011.9:g.8111787T>C , CM000673.1:g.8111787T>C	GRCh37
NC_000011.8:g.8068363T>C	NCBI36
NG_029912.1:g.56608T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.253+9T>C MANE Select	ENSP00000299506.3:n.253+9T>C
ENST00000299506.2:c.253+9T>C	ENSP00000299506.2:n.253+9T>C
ENST00000305253.8:c.418+9T>C	ENSP00000305426.4:n.418+9T>C
ENST00000534099.5:c.271+9T>C	ENSP00000434400.1:n.271+9T>C
NM_003320.4:c.418+9T>C	NP_003311.2:n.418+9T>C
NM_177972.2:c.253+9T>C	NP_813977.1:n.253+9T>C
XM_005253109.2:c.379+9T>C	XP_005253166.1:n.379+9T>C
XM_011520344.1:c.289+9T>C	XP_011518646.1:n.289+9T>C
XM_005253109.3:c.379+9T>C	XP_005253166.1:n.379+9T>C
XM_011520344.2:c.289+9T>C	XP_011518646.1:n.289+9T>C
NM_177972.3:c.253+9T>C MANE Select	NP_813977.1:n.253+9T>C
NM_003320.5:c.418+9T>C	NP_003311.2:n.418+9T>C