Canonical Allele Identifier: CA1950953332

Gene: TUB

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090101G= , CM000673.2:g.8090101G=	GRCh38
NC_000011.9:g.8111648G= , CM000673.1:g.8111648G=	GRCh37
NC_000011.8:g.8068224G=	NCBI36
NG_029912.1:g.56469G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.123G= MANE Select	ENSP00000299506.3:p.Lys41=
ENST00000299506.2:c.123G=	ENSP00000299506.2:p.Lys41=
ENST00000305253.8:c.288G=	ENSP00000305426.4:p.Lys96=
ENST00000534099.5:c.141G=	ENSP00000434400.1:p.Lys47=
NM_003320.4:c.288G=	NP_003311.2:p.Lys96=
NM_177972.2:c.123G=	NP_813977.1:p.Lys41=
XM_005253109.2:c.249G=	XP_005253166.1:p.Lys83=
XM_011520344.1:c.159G=	XP_011518646.1:p.Lys53=
XM_005253109.3:c.249G=	XP_005253166.1:p.Lys83=
XM_011520344.2:c.159G=	XP_011518646.1:p.Lys53=
NM_177972.3:c.123G= MANE Select	NP_813977.1:p.Lys41=
NM_003320.5:c.288G=	NP_003311.2:p.Lys96=