Canonical Allele Identifier: CA379562300

Gene: TUB

Linked Data

• gnomAD v4: 11-8089625-G-T
• MyVariant Identifiers: chr11:g.8111172G>T (hg19) ; chr11:g.8089625G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089625G>T , CM000673.2:g.8089625G>T	GRCh38
NC_000011.9:g.8111172G>T , CM000673.1:g.8111172G>T	GRCh37
NC_000011.8:g.8067748G>T	NCBI36
NG_029912.1:g.55993G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.54G>T MANE Select	ENSP00000299506.3:p.Glu18Asp
ENST00000299506.2:c.54G>T	ENSP00000299506.2:p.Glu18Asp
ENST00000305253.8:c.219G>T	ENSP00000305426.4:p.Glu73Asp
ENST00000534099.5:c.72G>T	ENSP00000434400.1:p.Glu24Asp
NM_003320.4:c.219G>T	NP_003311.2:p.Glu73Asp
NM_177972.2:c.54G>T	NP_813977.1:p.Glu18Asp
XM_005253109.2:c.180G>T	XP_005253166.1:p.Glu60Asp
XM_011520344.1:c.90G>T	XP_011518646.1:p.Glu30Asp
XM_005253109.3:c.180G>T	XP_005253166.1:p.Glu60Asp
XM_011520344.2:c.90G>T	XP_011518646.1:p.Glu30Asp
NM_177972.3:c.54G>T MANE Select	NP_813977.1:p.Glu18Asp
NM_003320.5:c.219G>T	NP_003311.2:p.Glu73Asp