Canonical Allele Identifier: CA217414966

Gene: TUB

Linked Data

• dbSNP Id: rs199620945
• MyVariant Identifiers: chr11:g.8111108_8111109del (hg19) ; chr11:g.8089561_8089562del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089561_8089562del , CM000673.2:g.8089561_8089562del	GRCh38
NC_000011.9:g.8111108_8111109del , CM000673.1:g.8111108_8111109del	GRCh37
NC_000011.8:g.8067684_8067685del	NCBI36
NG_029912.1:g.55929_55930del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-49_39-48del MANE Select	ENSP00000299506.3:n.39-49_39-48del
ENST00000299506.2:c.39-49_39-48del	ENSP00000299506.2:n.39-49_39-48del
ENST00000305253.8:c.204-49_204-48del	ENSP00000305426.4:n.204-49_204-48del
ENST00000534099.5:c.57-49_57-48del	ENSP00000434400.1:n.57-49_57-48del
NM_003320.4:c.204-49_204-48del	NP_003311.2:n.204-49_204-48del
NM_177972.2:c.39-49_39-48del	NP_813977.1:n.39-49_39-48del
XM_005253109.2:c.165-49_165-48del	XP_005253166.1:n.165-49_165-48del
XM_011520344.1:c.75-49_75-48del	XP_011518646.1:n.75-49_75-48del
XM_005253109.3:c.165-49_165-48del	XP_005253166.1:n.165-49_165-48del
XM_011520344.2:c.75-49_75-48del	XP_011518646.1:n.75-49_75-48del
NM_177972.3:c.39-49_39-48del MANE Select	NP_813977.1:n.39-49_39-48del
NM_003320.5:c.204-49_204-48del	NP_003311.2:n.204-49_204-48del