Canonical Allele Identifier: CA1618847642

Gene: TUBB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724178A= , CM000668.2:g.30724178A=	GRCh38
NC_000006.11:g.30691955A= , CM000668.1:g.30691955A=	GRCh37
NC_000006.10:g.30799934A=	NCBI36
NG_034142.1:g.8978A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1116A= MANE Select	ENSP00000339001.7:p.Thr372=
ENST00000680530.1:n.1978A=
ENST00000681421.1:n.2182A=
ENST00000681435.1:c.900A=	ENSP00000506665.1:p.Thr300=
ENST00000327892.12:c.1116A=	ENSP00000339001.7:p.Thr372=
ENST00000330914.7:c.900A=	ENSP00000365578.2:p.Thr300=
ENST00000396384.1:c.900A=	ENSP00000379668.1:p.Thr300=
ENST00000396389.5:c.1062A=	ENSP00000379672.1:p.Thr354=
NM_001293212.1:c.1176A=	NP_001280141.1:p.Thr392=
NM_001293213.1:c.510A=	NP_001280142.1:p.Thr170=
NM_001293214.1:c.984A=	NP_001280143.1:p.Thr328=
NM_001293215.1:c.900A=	NP_001280144.1:p.Thr300=
NM_001293216.1:c.900A=	NP_001280145.1:p.Thr300=
NM_178014.3:c.1116A=	NP_821133.1:p.Thr372=
NR_120608.1:n.823A=
NM_178014.4:c.1116A= MANE Select	NP_821133.1:p.Thr372=
NM_001293212.2:c.1176A=	NP_001280141.1:p.Thr392=
NM_001293213.2:c.510A=	NP_001280142.1:p.Thr170=
NM_001293214.2:c.984A=	NP_001280143.1:p.Thr328=
NM_001293215.2:c.900A=	NP_001280144.1:p.Thr300=
NM_001293216.2:c.900A=	NP_001280145.1:p.Thr300=
NR_120608.2:n.672A=