Canonical Allele Identifier: CA449777129
Gene: TUBB HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.30692015G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30724238G>A , CM000668.2:g.30724238G>A GRCh38
NC_000006.11:g.30692015G>A , CM000668.1:g.30692015G>A GRCh37
NC_000006.10:g.30799994G>A NCBI36
NG_034142.1:g.9038G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000327892.13:c.1176G>A MANE Select ENSP00000339001.7:p.Lys392=
ENST00000680530.1:n.2038G>A
ENST00000681421.1:n.2242G>A
ENST00000681435.1:c.960G>A ENSP00000506665.1:p.Lys320=
ENST00000327892.12:c.1176G>A ENSP00000339001.7:p.Lys392=
ENST00000330914.7:c.960G>A ENSP00000365578.2:p.Lys320=
ENST00000396384.1:c.960G>A ENSP00000379668.1:p.Lys320=
ENST00000396389.5:c.1122G>A ENSP00000379672.1:p.Lys374=
NM_001293212.1:c.1236G>A NP_001280141.1:p.Lys412=
NM_001293213.1:c.570G>A NP_001280142.1:p.Lys190=
NM_001293214.1:c.1044G>A NP_001280143.1:p.Lys348=
NM_001293215.1:c.960G>A NP_001280144.1:p.Lys320=
NM_001293216.1:c.960G>A NP_001280145.1:p.Lys320=
NM_178014.3:c.1176G>A NP_821133.1:p.Lys392=
NR_120608.1:n.883G>A
NM_178014.4:c.1176G>A MANE Select NP_821133.1:p.Lys392=
NM_001293212.2:c.1236G>A NP_001280141.1:p.Lys412=
NM_001293213.2:c.570G>A NP_001280142.1:p.Lys190=
NM_001293214.2:c.1044G>A NP_001280143.1:p.Lys348=
NM_001293215.2:c.960G>A NP_001280144.1:p.Lys320=
NM_001293216.2:c.960G>A NP_001280145.1:p.Lys320=
NR_120608.2:n.732G>A