Canonical Allele Identifier: CA7843908

Gene: TBC1D24

Linked Data

• ClinVar Variation Id: 646598
• ClinVar RCV Id: RCV000800917
• dbSNP Id: rs767293945
• ExAC: 16:2546177 G / A
• gnomAD v2: 16-2546177-G-A
• gnomAD v4: 16-2496176-G-A
• COSMIC: COSM4059580
• MyVariant Identifiers: chr16:g.2546177G>A (hg19) ; chr16:g.2496176G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2496176G>A , CM000678.2:g.2496176G>A	GRCh38
NC_000016.9:g.2546177G>A , CM000678.1:g.2546177G>A	GRCh37
NC_000016.8:g.2486178G>A	NCBI36
NG_028170.1:g.26031G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000562105.2:c.28G>A	ENSP00000457896.2:p.Val10Met
ENST00000567020.6:c.28G>A	ENSP00000454408.1:p.Val10Met
ENST00000569874.2:c.28G>A	ENSP00000455005.2:p.Val10Met
ENST00000643767.1:c.28G>A	ENSP00000494145.1:p.Val10Met
ENST00000646147.1:c.28G>A MANE Select	ENSP00000494678.1:p.Val10Met
ENST00000293970.9:c.28G>A	ENSP00000293970.5:p.Val10Met
ENST00000562105.1:c.28G>A	ENSP00000457896.1:p.Val10Met
ENST00000564543.1:c.28G>A	ENSP00000455547.1:p.Val10Met
ENST00000567020.5:c.28G>A	ENSP00000454408.1:p.Val10Met
ENST00000627285.1:c.28G>A	ENSP00000486121.1:p.Val10Met
ENST00000630263.2:c.28G>A	ENSP00000486835.1:p.Val10Met
NM_001199107.1:c.28G>A	NP_001186036.1:p.Val10Met
NM_020705.2:c.28G>A	NP_065756.1:p.Val10Met
XM_017023493.1:c.28G>A	XP_016878982.1:p.Val10Met
XM_017023494.1:c.28G>A	XP_016878983.1:p.Val10Met
XM_017023495.1:c.28G>A	XP_016878984.1:p.Val10Met
XR_001751956.1:n.210G>A
NM_001199107.2:c.28G>A MANE Select	NP_001186036.1:p.Val10Met
NM_020705.3:c.28G>A	NP_065756.1:p.Val10Met