Canonical Allele Identifier: CA1618847579

Gene: TUBB

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30723860T= , CM000668.2:g.30723860T=	GRCh38
NC_000006.11:g.30691637T= , CM000668.1:g.30691637T=	GRCh37
NC_000006.10:g.30799616T=	NCBI36
NG_034142.1:g.8660T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.798T= MANE Select	ENSP00000339001.7:p.Phe266=
ENST00000680530.1:n.1660T=
ENST00000681421.1:n.1864T=
ENST00000681435.1:c.582T=	ENSP00000506665.1:p.Phe194=
ENST00000327892.12:c.798T=	ENSP00000339001.7:p.Phe266=
ENST00000330914.7:c.582T=	ENSP00000365578.2:p.Phe194=
ENST00000396384.1:c.582T=	ENSP00000379668.1:p.Phe194=
ENST00000396389.5:c.744T=	ENSP00000379672.1:p.Phe248=
NM_001293212.1:c.858T=	NP_001280141.1:p.Phe286=
NM_001293213.1:c.370-178T=	NP_001280142.1:n.370-178T=
NM_001293214.1:c.666T=	NP_001280143.1:p.Phe222=
NM_001293215.1:c.582T=	NP_001280144.1:p.Phe194=
NM_001293216.1:c.582T=	NP_001280145.1:p.Phe194=
NM_178014.3:c.798T=	NP_821133.1:p.Phe266=
NR_120608.1:n.584-79T=
NM_178014.4:c.798T= MANE Select	NP_821133.1:p.Phe266=
NM_001293212.2:c.858T=	NP_001280141.1:p.Phe286=
NM_001293213.2:c.370-178T=	NP_001280142.1:n.370-178T=
NM_001293214.2:c.666T=	NP_001280143.1:p.Phe222=
NM_001293215.2:c.582T=	NP_001280144.1:p.Phe194=
NM_001293216.2:c.582T=	NP_001280145.1:p.Phe194=
NR_120608.2:n.433-79T=