Canonical Allele Identifier: CA10647239

Gene: TBC1D24

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2502436A>G , CM000678.2:g.2502436A>G	GRCh38
NC_000016.9:g.2552437A>G , CM000678.1:g.2552437A>G	GRCh37
NC_000016.8:g.2492438A>G	NCBI36
NG_028170.1:g.32291A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567020.6:c.*1478A>G	ENSP00000454408.1:n.*1478A>G
ENST00000569874.2:c.*821A>G	ENSP00000455005.2:n.*821A>G
ENST00000646147.1:c.*1478A>G MANE Select	ENSP00000494678.1:n.*1478A>G
ENST00000293970.9:c.*1478A>G	ENSP00000293970.5:n.*1478A>G
ENST00000564543.1:c.965+5323A>G	ENSP00000455547.1:n.965+5323A>G
ENST00000564879.2:c.2027A>G
ENST00000567020.5:c.*1478A>G	ENSP00000454408.1:n.*1478A>G
ENST00000627285.1:c.*1478A>G	ENSP00000486121.1:n.*1478A>G
ENST00000630263.2:c.*2116A>G	ENSP00000486835.1:n.*2116A>G
NM_001199107.1:c.*1478A>G	NP_001186036.1:n.*1478A>G
NM_020705.2:c.*1478A>G	NP_065756.1:n.*1478A>G
XM_017023493.1:c.*741A>G	XP_016878982.1:n.*741A>G
XM_017023494.1:c.*1478A>G	XP_016878983.1:n.*1478A>G
XM_017023495.1:c.*741A>G	XP_016878984.1:n.*741A>G
XR_001751956.1:n.3340A>G
NM_001199107.2:c.*1478A>G MANE Select	NP_001186036.1:n.*1478A>G
NM_020705.3:c.*1478A>G	NP_065756.1:n.*1478A>G