Canonical Allele Identifier: CA473009004

Gene: TUB

Linked Data

• gnomAD v4: 11-8089619-T-C
• MyVariant Identifiers: chr11:g.8111166T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089619T>C , CM000673.2:g.8089619T>C	GRCh38
NC_000011.9:g.8111166T>C , CM000673.1:g.8111166T>C	GRCh37
NC_000011.8:g.8067742T>C	NCBI36
NG_029912.1:g.55987T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.48T>C MANE Select	ENSP00000299506.3:p.Asp16=
ENST00000299506.2:c.48T>C	ENSP00000299506.2:p.Asp16=
ENST00000305253.8:c.213T>C	ENSP00000305426.4:p.Asp71=
ENST00000534099.5:c.66T>C	ENSP00000434400.1:p.Asp22=
NM_003320.4:c.213T>C	NP_003311.2:p.Asp71=
NM_177972.2:c.48T>C	NP_813977.1:p.Asp16=
XM_005253109.2:c.174T>C	XP_005253166.1:p.Asp58=
XM_011520344.1:c.84T>C	XP_011518646.1:p.Asp28=
XM_005253109.3:c.174T>C	XP_005253166.1:p.Asp58=
XM_011520344.2:c.84T>C	XP_011518646.1:p.Asp28=
NM_177972.3:c.48T>C MANE Select	NP_813977.1:p.Asp16=
NM_003320.5:c.213T>C	NP_003311.2:p.Asp71=