Canonical Allele Identifier: CA226205
Gene: GPR143 HGNC NCBI

Linked Data

ClinVar Variation Id: 98650
ClinVar RCV Id: RCV000084951 RCV001808320
dbSNP Id: rs281865184
gnomAD v4: X-9741337-C-T
MyVariant Identifiers: chrX:g.9709377C>T (hg19) chrX:g.9741337C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9741337C>T , CM000685.2:g.9741337C>T GRCh38
NC_000023.10:g.9709377C>T , CM000685.1:g.9709377C>T GRCh37
NC_000023.9:g.9669377C>T NCBI36
NG_009074.1:g.29541G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000467482.6:c.885+1G>A MANE Select ENSP00000417161.1:n.885+1G>A
ENST00000447366.5:c.633+1G>A ENSP00000390546.2:n.633+1G>A
ENST00000467482.5:c.885+1G>A ENSP00000417161.1:n.885+1G>A
NM_000273.2:c.885+1G>A NP_000264.2:n.885+1G>A
XM_005274541.2:c.885+1G>A XP_005274598.1:n.885+1G>A
XM_005274541.3:c.885+1G>A XP_005274598.1:n.885+1G>A
XM_024452387.1:c.633+1G>A XP_024308155.1:n.633+1G>A
XM_024452388.1:c.633+1G>A XP_024308156.1:n.633+1G>A
NM_000273.3:c.885+1G>A MANE Select NP_000264.2:n.885+1G>A
Search 100 bp 5'
Search 100 bp 3'