Canonical Allele Identifier: CA1950953586

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090211G= , CM000673.2:g.8090211G=	GRCh38
NC_000011.9:g.8111758G= , CM000673.1:g.8111758G=	GRCh37
NC_000011.8:g.8068334G=	NCBI36
NG_029912.1:g.56579G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.233G= MANE Select	ENSP00000299506.3:p.Ser78=
ENST00000299506.2:c.233G=	ENSP00000299506.2:p.Ser78=
ENST00000305253.8:c.398G=	ENSP00000305426.4:p.Ser133=
ENST00000534099.5:c.251G=	ENSP00000434400.1:p.Ser84=
NM_003320.4:c.398G=	NP_003311.2:p.Ser133=
NM_177972.2:c.233G=	NP_813977.1:p.Ser78=
XM_005253109.2:c.359G=	XP_005253166.1:p.Ser120=
XM_011520344.1:c.269G=	XP_011518646.1:p.Ser90=
XM_005253109.3:c.359G=	XP_005253166.1:p.Ser120=
XM_011520344.2:c.269G=	XP_011518646.1:p.Ser90=
NM_177972.3:c.233G= MANE Select	NP_813977.1:p.Ser78=
NM_003320.5:c.398G=	NP_003311.2:p.Ser133=