Canonical Allele Identifier: CA1950952641

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089560_8089562delinsATC , CM000673.2:g.8089560_8089562delinsATC	GRCh38
NC_000011.9:g.8111107_8111109delinsATC , CM000673.1:g.8111107_8111109delinsATC	GRCh37
NC_000011.8:g.8067683_8067685delinsATC	NCBI36
NG_029912.1:g.55928_55930delinsATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.39-50_39-48delinsATC MANE Select	ENSP00000299506.3:n.39-50_39-48delinsATC
ENST00000299506.2:c.39-50_39-48delinsATC	ENSP00000299506.2:n.39-50_39-48delinsATC
ENST00000305253.8:c.204-50_204-48delinsATC	ENSP00000305426.4:n.204-50_204-48delinsATC
ENST00000534099.5:c.57-50_57-48delinsATC	ENSP00000434400.1:n.57-50_57-48delinsATC
NM_003320.4:c.204-50_204-48delinsATC	NP_003311.2:n.204-50_204-48delinsATC
NM_177972.2:c.39-50_39-48delinsATC	NP_813977.1:n.39-50_39-48delinsATC
XM_005253109.2:c.165-50_165-48delinsATC	XP_005253166.1:n.165-50_165-48delinsATC
XM_011520344.1:c.75-50_75-48delinsATC	XP_011518646.1:n.75-50_75-48delinsATC
XM_005253109.3:c.165-50_165-48delinsATC	XP_005253166.1:n.165-50_165-48delinsATC
XM_011520344.2:c.75-50_75-48delinsATC	XP_011518646.1:n.75-50_75-48delinsATC
NM_177972.3:c.39-50_39-48delinsATC MANE Select	NP_813977.1:n.39-50_39-48delinsATC
NM_003320.5:c.204-50_204-48delinsATC	NP_003311.2:n.204-50_204-48delinsATC