Canonical Allele Identifier: CA379562597

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111632A>T (hg19) ; chr11:g.8090085A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090085A>T , CM000673.2:g.8090085A>T	GRCh38
NC_000011.9:g.8111632A>T , CM000673.1:g.8111632A>T	GRCh37
NC_000011.8:g.8068208A>T	NCBI36
NG_029912.1:g.56453A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.107A>T MANE Select	ENSP00000299506.3:p.Gln36Leu
ENST00000299506.2:c.107A>T	ENSP00000299506.2:p.Gln36Leu
ENST00000305253.8:c.272A>T	ENSP00000305426.4:p.Gln91Leu
ENST00000534099.5:c.125A>T	ENSP00000434400.1:p.Gln42Leu
NM_003320.4:c.272A>T	NP_003311.2:p.Gln91Leu
NM_177972.2:c.107A>T	NP_813977.1:p.Gln36Leu
XM_005253109.2:c.233A>T	XP_005253166.1:p.Gln78Leu
XM_011520344.1:c.143A>T	XP_011518646.1:p.Gln48Leu
XM_005253109.3:c.233A>T	XP_005253166.1:p.Gln78Leu
XM_011520344.2:c.143A>T	XP_011518646.1:p.Gln48Leu
NM_177972.3:c.107A>T MANE Select	NP_813977.1:p.Gln36Leu
NM_003320.5:c.272A>T	NP_003311.2:p.Gln91Leu