Canonical Allele Identifier: CA10637439

Gene: TBC1D24

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2501829G>A , CM000678.2:g.2501829G>A	GRCh38
NC_000016.9:g.2551830G>A , CM000678.1:g.2551830G>A	GRCh37
NC_000016.8:g.2491831G>A	NCBI36
NG_028170.1:g.31684G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567020.6:c.*871G>A	ENSP00000454408.1:n.*871G>A
ENST00000569874.2:c.*214G>A	ENSP00000455005.2:n.*214G>A
ENST00000646147.1:c.*871G>A MANE Select	ENSP00000494678.1:n.*871G>A
ENST00000293970.9:c.*871G>A	ENSP00000293970.5:n.*871G>A
ENST00000564543.1:c.965+4716G>A	ENSP00000455547.1:n.965+4716G>A
ENST00000564879.2:c.1420G>A
ENST00000567020.5:c.*871G>A	ENSP00000454408.1:n.*871G>A
ENST00000569874.1:c.274G>A	ENSP00000455005.1:n.274G>A
ENST00000627285.1:c.*871G>A	ENSP00000486121.1:n.*871G>A
ENST00000630263.2:c.*1509G>A	ENSP00000486835.1:n.*1509G>A
NM_001199107.1:c.*871G>A	NP_001186036.1:n.*871G>A
NM_020705.2:c.*871G>A	NP_065756.1:n.*871G>A
XM_017023493.1:c.*134G>A	XP_016878982.1:n.*134G>A
XM_017023494.1:c.*871G>A	XP_016878983.1:n.*871G>A
XM_017023495.1:c.*134G>A	XP_016878984.1:n.*134G>A
XR_001751956.1:n.2733G>A
NM_001199107.2:c.*871G>A MANE Select	NP_001186036.1:n.*871G>A
NM_020705.3:c.*871G>A	NP_065756.1:n.*871G>A