Canonical Allele Identifier: CA363150689

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691930C>A (hg19) ; chr6:g.30724153C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724153C>A , CM000668.2:g.30724153C>A	GRCh38
NC_000006.11:g.30691930C>A , CM000668.1:g.30691930C>A	GRCh37
NC_000006.10:g.30799909C>A	NCBI36
NG_034142.1:g.8953C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1091C>A MANE Select	ENSP00000339001.7:p.Ala364Glu
ENST00000680530.1:n.1953C>A
ENST00000681421.1:n.2157C>A
ENST00000681435.1:c.875C>A	ENSP00000506665.1:p.Ala292Glu
ENST00000327892.12:c.1091C>A	ENSP00000339001.7:p.Ala364Glu
ENST00000330914.7:c.875C>A	ENSP00000365578.2:p.Ala292Glu
ENST00000396384.1:c.875C>A	ENSP00000379668.1:p.Ala292Glu
ENST00000396389.5:c.1037C>A	ENSP00000379672.1:p.Ala346Glu
NM_001293212.1:c.1151C>A	NP_001280141.1:p.Ala384Glu
NM_001293213.1:c.485C>A	NP_001280142.1:p.Ala162Glu
NM_001293214.1:c.959C>A	NP_001280143.1:p.Ala320Glu
NM_001293215.1:c.875C>A	NP_001280144.1:p.Ala292Glu
NM_001293216.1:c.875C>A	NP_001280145.1:p.Ala292Glu
NM_178014.3:c.1091C>A	NP_821133.1:p.Ala364Glu
NR_120608.1:n.798C>A
NM_178014.4:c.1091C>A MANE Select	NP_821133.1:p.Ala364Glu
NM_001293212.2:c.1151C>A	NP_001280141.1:p.Ala384Glu
NM_001293213.2:c.485C>A	NP_001280142.1:p.Ala162Glu
NM_001293214.2:c.959C>A	NP_001280143.1:p.Ala320Glu
NM_001293215.2:c.875C>A	NP_001280144.1:p.Ala292Glu
NM_001293216.2:c.875C>A	NP_001280145.1:p.Ala292Glu
NR_120608.2:n.647C>A