Canonical Allele Identifier: CA363151665

Gene: TUBB

Linked Data

• MyVariant Identifiers: chr6:g.30692070G>T (hg19) ; chr6:g.30724293G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.30724293G>T , CM000668.2:g.30724293G>T	GRCh38
NC_000006.11:g.30692070G>T , CM000668.1:g.30692070G>T	GRCh37
NC_000006.10:g.30800049G>T	NCBI36
NG_034142.1:g.9093G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327892.13:c.1231G>T MANE Select	ENSP00000339001.7:p.Ala411Ser
ENST00000680530.1:n.2093G>T
ENST00000681421.1:n.2297G>T
ENST00000681435.1:c.1015G>T	ENSP00000506665.1:p.Ala339Ser
ENST00000327892.12:c.1231G>T	ENSP00000339001.7:p.Ala411Ser
ENST00000330914.7:c.1015G>T	ENSP00000365578.2:p.Ala339Ser
ENST00000396384.1:c.1015G>T	ENSP00000379668.1:p.Ala339Ser
ENST00000396389.5:c.1177G>T	ENSP00000379672.1:p.Ala393Ser
NM_001293212.1:c.1291G>T	NP_001280141.1:p.Ala431Ser
NM_001293213.1:c.625G>T	NP_001280142.1:p.Ala209Ser
NM_001293214.1:c.1099G>T	NP_001280143.1:p.Ala367Ser
NM_001293215.1:c.1015G>T	NP_001280144.1:p.Ala339Ser
NM_001293216.1:c.1015G>T	NP_001280145.1:p.Ala339Ser
NM_178014.3:c.1231G>T	NP_821133.1:p.Ala411Ser
NR_120608.1:n.938G>T
NM_178014.4:c.1231G>T MANE Select	NP_821133.1:p.Ala411Ser
NM_001293212.2:c.1291G>T	NP_001280141.1:p.Ala431Ser
NM_001293213.2:c.625G>T	NP_001280142.1:p.Ala209Ser
NM_001293214.2:c.1099G>T	NP_001280143.1:p.Ala367Ser
NM_001293215.2:c.1015G>T	NP_001280144.1:p.Ala339Ser
NM_001293216.2:c.1015G>T	NP_001280145.1:p.Ala339Ser
NR_120608.2:n.787G>T