Canonical Allele Identifier: CA10637435

Gene: TBC1D24

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2501794C>T , CM000678.2:g.2501794C>T	GRCh38
NC_000016.9:g.2551795C>T , CM000678.1:g.2551795C>T	GRCh37
NC_000016.8:g.2491796C>T	NCBI36
NG_028170.1:g.31649C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567020.6:c.*836C>T	ENSP00000454408.1:n.*836C>T
ENST00000569874.2:c.*179C>T	ENSP00000455005.2:n.*179C>T
ENST00000646147.1:c.*836C>T MANE Select	ENSP00000494678.1:n.*836C>T
ENST00000293970.9:c.*836C>T	ENSP00000293970.5:n.*836C>T
ENST00000564543.1:c.965+4681C>T	ENSP00000455547.1:n.965+4681C>T
ENST00000564879.2:c.1385C>T
ENST00000567020.5:c.*836C>T	ENSP00000454408.1:n.*836C>T
ENST00000569874.1:c.239C>T	ENSP00000455005.1:n.239C>T
ENST00000627285.1:c.*836C>T	ENSP00000486121.1:n.*836C>T
ENST00000630263.2:c.*1474C>T	ENSP00000486835.1:n.*1474C>T
NM_001199107.1:c.*836C>T	NP_001186036.1:n.*836C>T
NM_020705.2:c.*836C>T	NP_065756.1:n.*836C>T
XM_017023493.1:c.*99C>T	XP_016878982.1:n.*99C>T
XM_017023494.1:c.*836C>T	XP_016878983.1:n.*836C>T
XM_017023495.1:c.*99C>T	XP_016878984.1:n.*99C>T
XR_001751956.1:n.2698C>T
NM_001199107.2:c.*836C>T MANE Select	NP_001186036.1:n.*836C>T
NM_020705.3:c.*836C>T	NP_065756.1:n.*836C>T