Canonical Allele Identifier: CA384645116
Gene: TUBA1A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49186685G>T , CM000674.2:g.49186685G>T GRCh38
NC_000012.11:g.49580468G>T , CM000674.1:g.49580468G>T GRCh37
NC_000012.10:g.47866735G>T NCBI36
NG_008966.1:g.7394C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301071.12:c.152C>A MANE Select ENSP00000301071.7:p.Thr51Asn
ENST00000547939.6:c.47C>A ENSP00000450268.2:p.Thr16Asn
ENST00000550767.6:c.47C>A ENSP00000446637.1:p.Thr16Asn
ENST00000550811.2:n.1185C>A
ENST00000552924.2:c.47C>A ENSP00000448725.2:p.Thr16Asn
ENST00000679733.1:c.152C>A ENSP00000505459.1:p.Thr51Asn
ENST00000295766.9:c.152C>A ENSP00000439020.2:p.Thr51Asn
ENST00000301071.11:c.152C>A ENSP00000301071.7:p.Thr51Asn
ENST00000546918.1:c.152C>A ENSP00000446613.1:p.Thr51Asn
ENST00000547939.5:c.47C>A ENSP00000450268.1:p.Thr16Asn
ENST00000548363.1:n.156C>A
ENST00000550254.1:n.174C>A
ENST00000550767.5:c.47C>A ENSP00000446637.1:p.Thr16Asn
ENST00000550811.1:c.47C>A ENSP00000449016.1:p.Thr16Asn
ENST00000552924.1:c.47C>A ENSP00000448725.1:p.Thr16Asn
NM_001270399.1:c.152C>A NP_001257328.1:p.Thr51Asn
NM_001270400.1:c.47C>A NP_001257329.1:p.Thr16Asn
NM_006009.3:c.152C>A NP_006000.2:p.Thr51Asn
NM_006009.4:c.152C>A MANE Select NP_006000.2:p.Thr51Asn
NM_001270399.2:c.152C>A NP_001257328.1:p.Thr51Asn
NM_001270400.2:c.47C>A NP_001257329.1:p.Thr16Asn