Canonical Allele Identifier: CA16608138
Gene: TBC1D24 HGNC NCBI

Linked Data

ClinVar Variation Id: 391688
ClinVar RCV Id: RCV000418994 RCV001049900
dbSNP Id: rs1057524192
gnomAD v4: 16-2496469-T-A
MyVariant Identifiers: chr16:g.2546470T>A (hg19) chr16:g.2496469T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2496469T>A , CM000678.2:g.2496469T>A GRCh38
NC_000016.9:g.2546470T>A , CM000678.1:g.2546470T>A GRCh37
NC_000016.8:g.2486471T>A NCBI36
NG_028170.1:g.26324T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000562105.2:c.321T>A ENSP00000457896.2:p.Asn107Lys
ENST00000567020.6:c.321T>A ENSP00000454408.1:p.Asn107Lys
ENST00000569874.2:c.321T>A ENSP00000455005.2:p.Asn107Lys
ENST00000643767.1:c.321T>A ENSP00000494145.1:p.Asn107Lys
ENST00000646147.1:c.321T>A MANE Select ENSP00000494678.1:p.Asn107Lys
ENST00000293970.9:c.321T>A ENSP00000293970.5:p.Asn107Lys
ENST00000564543.1:c.321T>A ENSP00000455547.1:p.Asn107Lys
ENST00000567020.5:c.321T>A ENSP00000454408.1:p.Asn107Lys
ENST00000627285.1:c.321T>A ENSP00000486121.1:p.Asn107Lys
ENST00000630263.2:c.321T>A ENSP00000486835.1:p.Asn107Lys
NM_001199107.1:c.321T>A NP_001186036.1:p.Asn107Lys
NM_020705.2:c.321T>A NP_065756.1:p.Asn107Lys
XM_017023493.1:c.321T>A XP_016878982.1:p.Asn107Lys
XM_017023494.1:c.321T>A XP_016878983.1:p.Asn107Lys
XM_017023495.1:c.321T>A XP_016878984.1:p.Asn107Lys
XR_001751956.1:n.503T>A
NM_001199107.2:c.321T>A MANE Select NP_001186036.1:p.Asn107Lys
NM_020705.3:c.321T>A NP_065756.1:p.Asn107Lys
Search 100 bp 5'
Search 100 bp 3'