Canonical Allele Identifier: CA363151745

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30692085A>C (hg19) ; chr6:g.30724308A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724308A>C , CM000668.2:g.30724308A>C	GRCh38
NC_000006.11:g.30692085A>C , CM000668.1:g.30692085A>C	GRCh37
NC_000006.10:g.30800064A>C	NCBI36
NG_034142.1:g.9108A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1246A>C MANE Select	ENSP00000339001.7:p.Asn416His
ENST00000680530.1:n.2108A>C
ENST00000681421.1:n.2312A>C
ENST00000681435.1:c.1030A>C	ENSP00000506665.1:p.Asn344His
ENST00000327892.12:c.1246A>C	ENSP00000339001.7:p.Asn416His
ENST00000330914.7:c.1030A>C	ENSP00000365578.2:p.Asn344His
ENST00000396384.1:c.1030A>C	ENSP00000379668.1:p.Asn344His
ENST00000396389.5:c.1192A>C	ENSP00000379672.1:p.Asn398His
NM_001293212.1:c.1306A>C	NP_001280141.1:p.Asn436His
NM_001293213.1:c.640A>C	NP_001280142.1:p.Asn214His
NM_001293214.1:c.1114A>C	NP_001280143.1:p.Asn372His
NM_001293215.1:c.1030A>C	NP_001280144.1:p.Asn344His
NM_001293216.1:c.1030A>C	NP_001280145.1:p.Asn344His
NM_178014.3:c.1246A>C	NP_821133.1:p.Asn416His
NR_120608.1:n.953A>C
NM_178014.4:c.1246A>C MANE Select	NP_821133.1:p.Asn416His
NM_001293212.2:c.1306A>C	NP_001280141.1:p.Asn436His
NM_001293213.2:c.640A>C	NP_001280142.1:p.Asn214His
NM_001293214.2:c.1114A>C	NP_001280143.1:p.Asn372His
NM_001293215.2:c.1030A>C	NP_001280144.1:p.Asn344His
NM_001293216.2:c.1030A>C	NP_001280145.1:p.Asn344His
NR_120608.2:n.802A>C