Canonical Allele Identifier: CA10648178

Gene: TBC1D24

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2501345T>C , CM000678.2:g.2501345T>C	GRCh38
NC_000016.9:g.2551346T>C , CM000678.1:g.2551346T>C	GRCh37
NC_000016.8:g.2491347T>C	NCBI36
NG_028170.1:g.31200T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567020.6:c.*387T>C	ENSP00000454408.1:n.*387T>C
ENST00000569874.2:c.*94+293T>C	ENSP00000455005.2:n.*94+293T>C
ENST00000646147.1:c.*387T>C MANE Select	ENSP00000494678.1:n.*387T>C
ENST00000293970.9:c.*387T>C	ENSP00000293970.5:n.*387T>C
ENST00000564543.1:c.965+4232T>C	ENSP00000455547.1:n.965+4232T>C
ENST00000564879.2:c.936T>C
ENST00000567020.5:c.*387T>C	ENSP00000454408.1:n.*387T>C
ENST00000569874.1:c.154+293T>C	ENSP00000455005.1:n.154+293T>C
ENST00000627285.1:c.*387T>C	ENSP00000486121.1:n.*387T>C
ENST00000630263.2:c.*1025T>C	ENSP00000486835.1:n.*1025T>C
NM_001199107.1:c.*387T>C	NP_001186036.1:n.*387T>C
NM_020705.2:c.*387T>C	NP_065756.1:n.*387T>C
XM_017023493.1:c.*15-365T>C	XP_016878982.1:n.*15-365T>C
XM_017023494.1:c.*387T>C	XP_016878983.1:n.*387T>C
XM_017023495.1:c.*15-365T>C	XP_016878984.1:n.*15-365T>C
XR_001751956.1:n.2249T>C
NM_001199107.2:c.*387T>C MANE Select	NP_001186036.1:n.*387T>C
NM_020705.3:c.*387T>C	NP_065756.1:n.*387T>C