Canonical Allele Identifier: CA2202261293

Gene: TBC1D24

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2499425G>C , CM000678.2:g.2499425G>C	GRCh38
NC_000016.9:g.2549426G>C , CM000678.1:g.2549426G>C	GRCh37
NC_000016.8:g.2489427G>C	NCBI36
NG_028170.1:g.29280G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000562105.2:c.1206+5G>C	ENSP00000457896.2:n.1206+5G>C
ENST00000567020.6:c.1188+5G>C	ENSP00000454408.1:n.1188+5G>C
ENST00000569874.2:c.1188+5G>C	ENSP00000455005.2:n.1188+5G>C
ENST00000643767.1:c.1188+5G>C	ENSP00000494145.1:n.1188+5G>C
ENST00000646147.1:c.1206+5G>C MANE Select	ENSP00000494678.1:n.1206+5G>C
ENST00000293970.9:c.1206+5G>C	ENSP00000293970.5:n.1206+5G>C
ENST00000564543.1:c.965+2312G>C	ENSP00000455547.1:n.965+2312G>C
ENST00000564879.2:c.76-410G>C
ENST00000567020.5:c.1188+5G>C	ENSP00000454408.1:n.1188+5G>C
ENST00000627285.1:c.1188+5G>C	ENSP00000486121.1:n.1188+5G>C
ENST00000630263.2:c.*164+5G>C	ENSP00000486835.1:n.*164+5G>C
NM_001199107.1:c.1206+5G>C	NP_001186036.1:n.1206+5G>C
NM_020705.2:c.1188+5G>C	NP_065756.1:n.1188+5G>C
XM_017023493.1:c.1206+5G>C	XP_016878982.1:n.1206+5G>C
XM_017023494.1:c.1188+5G>C	XP_016878983.1:n.1188+5G>C
XM_017023495.1:c.1188+5G>C	XP_016878984.1:n.1188+5G>C
XR_001751956.1:n.1388+5G>C
NM_001199107.2:c.1206+5G>C MANE Select	NP_001186036.1:n.1206+5G>C
NM_020705.3:c.1188+5G>C	NP_065756.1:n.1188+5G>C