Canonical Allele Identifier: CA16043601
Gene: GPR143 HGNC NCBI

Linked Data

ClinVar Variation Id: 373941
ClinVar RCV Id: RCV000414936 RCV002291275 RCV002521446
dbSNP Id: rs1057518787
MyVariant Identifiers: chrX:g.9733822_9733846del (hg19) chrX:g.9765782_9765806del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765786_9765810del , CM000685.2:g.9765786_9765810del GRCh38
NC_000023.10:g.9733826_9733850del , CM000685.1:g.9733826_9733850del GRCh37
NC_000023.9:g.9693826_9693850del NCBI36
NG_009074.1:g.5072_5096del

Transcript Alleles

HGVS Amino-acid change
ENST00000467482.6:c.12_36del MANE Select ENSP00000417161.1:p.Leu6GlyfsTer9
ENST00000431126.1:c.-3+314_-3+338del ENSP00000406138.1:n.-3+314_-3+338del
ENST00000447366.5:c.-2-4980_-2-4956del ENSP00000390546.2:n.-2-4980_-2-4956del
ENST00000467482.5:c.12_36del ENSP00000417161.1:p.Leu6GlyfsTer9
NM_000273.2:c.12_36del NP_000264.2:p.Leu6GlyfsTer9
XM_005274541.2:c.12_36del XP_005274598.1:p.Leu6GlyfsTer9
XM_005274541.3:c.12_36del XP_005274598.1:p.Leu6GlyfsTer9
XM_024452387.1:c.-2-4980_-2-4956del XP_024308155.1:n.-2-4980_-2-4956del
XM_024452388.1:c.-2-4980_-2-4956del XP_024308156.1:n.-2-4980_-2-4956del
NM_000273.3:c.12_36del MANE Select NP_000264.2:p.Leu6GlyfsTer9
Search 100 bp 5'
Search 100 bp 3'