Canonical Allele Identifier: CA2618625435

Gene: TUBA1A

Linked Data

• gnomAD v4: 12-49187001-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49187002del , CM000674.2:g.49187002del	GRCh38
NC_000012.11:g.49580785del , CM000674.1:g.49580785del	GRCh37
NC_000012.10:g.47867052del	NCBI36
NG_008966.1:g.7077del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.4-169del MANE Select	ENSP00000301071.7:n.4-169del
ENST00000547939.6:c.-115del	ENSP00000450268.2:n.-115del
ENST00000550767.6:c.-115del	ENSP00000446637.1:n.-115del
ENST00000550811.2:n.868del
ENST00000552924.2:c.-102-169del	ENSP00000448725.2:n.-102-169del
ENST00000679733.1:c.4-169del	ENSP00000505459.1:n.4-169del
ENST00000295766.9:c.4-169del	ENSP00000439020.2:n.4-169del
ENST00000301071.11:c.4-169del	ENSP00000301071.7:n.4-169del
ENST00000546918.1:c.4-169del	ENSP00000446613.1:n.4-169del
ENST00000547939.5:c.-115del	ENSP00000450268.1:n.-115del
ENST00000548363.1:n.8-169del
ENST00000550254.1:n.26-169del
ENST00000550811.1:c.-115del	ENSP00000449016.1:n.-115del
ENST00000552924.1:c.-102-169del	ENSP00000448725.1:n.-102-169del
NM_001270399.1:c.4-169del	NP_001257328.1:n.4-169del
NM_001270400.1:c.-102-169del	NP_001257329.1:n.-102-169del
NM_006009.3:c.4-169del	NP_006000.2:n.4-169del
NM_006009.4:c.4-169del MANE Select	NP_006000.2:n.4-169del
NM_001270399.2:c.4-169del	NP_001257328.1:n.4-169del
NM_001270400.2:c.-102-169del	NP_001257329.1:n.-102-169del