Canonical Allele Identifier: CA363150185

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30691864T>C (hg19) ; chr6:g.30724087T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724087T>C , CM000668.2:g.30724087T>C	GRCh38
NC_000006.11:g.30691864T>C , CM000668.1:g.30691864T>C	GRCh37
NC_000006.10:g.30799843T>C	NCBI36
NG_034142.1:g.8887T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1025T>C MANE Select	ENSP00000339001.7:p.Val342Ala
ENST00000680530.1:n.1887T>C
ENST00000681421.1:n.2091T>C
ENST00000681435.1:c.809T>C	ENSP00000506665.1:p.Val270Ala
ENST00000327892.12:c.1025T>C	ENSP00000339001.7:p.Val342Ala
ENST00000330914.7:c.809T>C	ENSP00000365578.2:p.Val270Ala
ENST00000396384.1:c.809T>C	ENSP00000379668.1:p.Val270Ala
ENST00000396389.5:c.971T>C	ENSP00000379672.1:p.Val324Ala
NM_001293212.1:c.1085T>C	NP_001280141.1:p.Val362Ala
NM_001293213.1:c.419T>C	NP_001280142.1:p.Val140Ala
NM_001293214.1:c.893T>C	NP_001280143.1:p.Val298Ala
NM_001293215.1:c.809T>C	NP_001280144.1:p.Val270Ala
NM_001293216.1:c.809T>C	NP_001280145.1:p.Val270Ala
NM_178014.3:c.1025T>C	NP_821133.1:p.Val342Ala
NR_120608.1:n.732T>C
NM_178014.4:c.1025T>C MANE Select	NP_821133.1:p.Val342Ala
NM_001293212.2:c.1085T>C	NP_001280141.1:p.Val362Ala
NM_001293213.2:c.419T>C	NP_001280142.1:p.Val140Ala
NM_001293214.2:c.893T>C	NP_001280143.1:p.Val298Ala
NM_001293215.2:c.809T>C	NP_001280144.1:p.Val270Ala
NM_001293216.2:c.809T>C	NP_001280145.1:p.Val270Ala
NR_120608.2:n.581T>C