Canonical Allele Identifier: CA449777011

Gene: TUBB

Linked Data

• COSMIC: COSM3252074
• MyVariant Identifiers: chr6:g.30691949T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724172T>C , CM000668.2:g.30724172T>C	GRCh38
NC_000006.11:g.30691949T>C , CM000668.1:g.30691949T>C	GRCh37
NC_000006.10:g.30799928T>C	NCBI36
NG_034142.1:g.8972T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1110T>C MANE Select	ENSP00000339001.7:p.Asn370=
ENST00000680530.1:n.1972T>C
ENST00000681421.1:n.2176T>C
ENST00000681435.1:c.894T>C	ENSP00000506665.1:p.Asn298=
ENST00000327892.12:c.1110T>C	ENSP00000339001.7:p.Asn370=
ENST00000330914.7:c.894T>C	ENSP00000365578.2:p.Asn298=
ENST00000396384.1:c.894T>C	ENSP00000379668.1:p.Asn298=
ENST00000396389.5:c.1056T>C	ENSP00000379672.1:p.Asn352=
NM_001293212.1:c.1170T>C	NP_001280141.1:p.Asn390=
NM_001293213.1:c.504T>C	NP_001280142.1:p.Asn168=
NM_001293214.1:c.978T>C	NP_001280143.1:p.Asn326=
NM_001293215.1:c.894T>C	NP_001280144.1:p.Asn298=
NM_001293216.1:c.894T>C	NP_001280145.1:p.Asn298=
NM_178014.3:c.1110T>C	NP_821133.1:p.Asn370=
NR_120608.1:n.817T>C
NM_178014.4:c.1110T>C MANE Select	NP_821133.1:p.Asn370=
NM_001293212.2:c.1170T>C	NP_001280141.1:p.Asn390=
NM_001293213.2:c.504T>C	NP_001280142.1:p.Asn168=
NM_001293214.2:c.978T>C	NP_001280143.1:p.Asn326=
NM_001293215.2:c.894T>C	NP_001280144.1:p.Asn298=
NM_001293216.2:c.894T>C	NP_001280145.1:p.Asn298=
NR_120608.2:n.666T>C