Canonical Allele Identifier: CA1950953569

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090197_8090202delinsCTACCT , CM000673.2:g.8090197_8090202delinsCTACCT	GRCh38
NC_000011.9:g.8111744_8111749delinsCTACCT , CM000673.1:g.8111744_8111749delinsCTACCT	GRCh37
NC_000011.8:g.8068320_8068325delinsCTACCT	NCBI36
NG_029912.1:g.56565_56570delinsCTACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.219_224delinsCTACCT MANE Select	ENSP00000299506.3:p.Ser73=
ENST00000299506.2:c.219_224delinsCTACCT	ENSP00000299506.2:p.Ser73=
ENST00000305253.8:c.384_389delinsCTACCT	ENSP00000305426.4:p.Ser128=
ENST00000534099.5:c.237_242delinsCTACCT	ENSP00000434400.1:p.Ser79=
NM_003320.4:c.384_389delinsCTACCT	NP_003311.2:p.Ser128=
NM_177972.2:c.219_224delinsCTACCT	NP_813977.1:p.Ser73=
XM_005253109.2:c.345_350delinsCTACCT	XP_005253166.1:p.Ser115=
XM_011520344.1:c.255_260delinsCTACCT	XP_011518646.1:p.Ser85=
XM_005253109.3:c.345_350delinsCTACCT	XP_005253166.1:p.Ser115=
XM_011520344.2:c.255_260delinsCTACCT	XP_011518646.1:p.Ser85=
NM_177972.3:c.219_224delinsCTACCT MANE Select	NP_813977.1:p.Ser73=
NM_003320.5:c.384_389delinsCTACCT	NP_003311.2:p.Ser128=