Canonical Allele Identifier: CA1618847622

Gene: TUBB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724088G= , CM000668.2:g.30724088G=	GRCh38
NC_000006.11:g.30691865G= , CM000668.1:g.30691865G=	GRCh37
NC_000006.10:g.30799844G=	NCBI36
NG_034142.1:g.8888G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1026G= MANE Select	ENSP00000339001.7:p.Val342=
ENST00000680530.1:n.1888G=
ENST00000681421.1:n.2092G=
ENST00000681435.1:c.810G=	ENSP00000506665.1:p.Val270=
ENST00000327892.12:c.1026G=	ENSP00000339001.7:p.Val342=
ENST00000330914.7:c.810G=	ENSP00000365578.2:p.Val270=
ENST00000396384.1:c.810G=	ENSP00000379668.1:p.Val270=
ENST00000396389.5:c.972G=	ENSP00000379672.1:p.Val324=
NM_001293212.1:c.1086G=	NP_001280141.1:p.Val362=
NM_001293213.1:c.420G=	NP_001280142.1:p.Val140=
NM_001293214.1:c.894G=	NP_001280143.1:p.Val298=
NM_001293215.1:c.810G=	NP_001280144.1:p.Val270=
NM_001293216.1:c.810G=	NP_001280145.1:p.Val270=
NM_178014.3:c.1026G=	NP_821133.1:p.Val342=
NR_120608.1:n.733G=
NM_178014.4:c.1026G= MANE Select	NP_821133.1:p.Val342=
NM_001293212.2:c.1086G=	NP_001280141.1:p.Val362=
NM_001293213.2:c.420G=	NP_001280142.1:p.Val140=
NM_001293214.2:c.894G=	NP_001280143.1:p.Val298=
NM_001293215.2:c.810G=	NP_001280144.1:p.Val270=
NM_001293216.2:c.810G=	NP_001280145.1:p.Val270=
NR_120608.2:n.582G=