Canonical Allele Identifier: CA1950953604

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090227C= , CM000673.2:g.8090227C=	GRCh38
NC_000011.9:g.8111774C= , CM000673.1:g.8111774C=	GRCh37
NC_000011.8:g.8068350C=	NCBI36
NG_029912.1:g.56595C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.249C= MANE Select	ENSP00000299506.3:p.Tyr83=
ENST00000299506.2:c.249C=	ENSP00000299506.2:p.Tyr83=
ENST00000305253.8:c.414C=	ENSP00000305426.4:p.Tyr138=
ENST00000534099.5:c.267C=	ENSP00000434400.1:p.Tyr89=
NM_003320.4:c.414C=	NP_003311.2:p.Tyr138=
NM_177972.2:c.249C=	NP_813977.1:p.Tyr83=
XM_005253109.2:c.375C=	XP_005253166.1:p.Tyr125=
XM_011520344.1:c.285C=	XP_011518646.1:p.Tyr95=
XM_005253109.3:c.375C=	XP_005253166.1:p.Tyr125=
XM_011520344.2:c.285C=	XP_011518646.1:p.Tyr95=
NM_177972.3:c.249C= MANE Select	NP_813977.1:p.Tyr83=
NM_003320.5:c.414C=	NP_003311.2:p.Tyr138=