Canonical Allele Identifier: CA1950953290

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090084C= , CM000673.2:g.8090084C=	GRCh38
NC_000011.9:g.8111631C= , CM000673.1:g.8111631C=	GRCh37
NC_000011.8:g.8068207C=	NCBI36
NG_029912.1:g.56452C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.106C= MANE Select	ENSP00000299506.3:p.Gln36=
ENST00000299506.2:c.106C=	ENSP00000299506.2:p.Gln36=
ENST00000305253.8:c.271C=	ENSP00000305426.4:p.Gln91=
ENST00000534099.5:c.124C=	ENSP00000434400.1:p.Gln42=
NM_003320.4:c.271C=	NP_003311.2:p.Gln91=
NM_177972.2:c.106C=	NP_813977.1:p.Gln36=
XM_005253109.2:c.232C=	XP_005253166.1:p.Gln78=
XM_011520344.1:c.142C=	XP_011518646.1:p.Gln48=
XM_005253109.3:c.232C=	XP_005253166.1:p.Gln78=
XM_011520344.2:c.142C=	XP_011518646.1:p.Gln48=
NM_177972.3:c.106C= MANE Select	NP_813977.1:p.Gln36=
NM_003320.5:c.271C=	NP_003311.2:p.Gln91=