Canonical Allele Identifier: CA10345091
Gene: GPR143 HGNC NCBI

Linked Data

ClinVar Variation Id: 1638735
ClinVar RCV Id: RCV002126400
dbSNP Id: rs751927343
ExAC: X:9733777 C / T
gnomAD v2: X-9733777-C-T
gnomAD v3: X-9765737-C-T
gnomAD v4: X-9765737-C-T
MyVariant Identifiers: chrX:g.9733777C>T (hg19) chrX:g.9765737C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765737C>T , CM000685.2:g.9765737C>T GRCh38
NC_000023.10:g.9733777C>T , CM000685.1:g.9733777C>T GRCh37
NC_000023.9:g.9693777C>T NCBI36
NG_009074.1:g.5141G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.81G>A MANE Select ENSP00000417161.1:p.Arg27=
ENST00000431126.1:c.-3+383G>A ENSP00000406138.1:n.-3+383G>A
ENST00000447366.5:c.-2-4911G>A ENSP00000390546.2:n.-2-4911G>A
ENST00000467482.5:c.81G>A ENSP00000417161.1:p.Arg27=
NM_000273.2:c.81G>A NP_000264.2:p.Arg27=
XM_005274541.2:c.81G>A XP_005274598.1:p.Arg27=
XM_005274541.3:c.81G>A XP_005274598.1:p.Arg27=
XM_024452387.1:c.-2-4911G>A XP_024308155.1:n.-2-4911G>A
XM_024452388.1:c.-2-4911G>A XP_024308156.1:n.-2-4911G>A
NM_000273.3:c.81G>A MANE Select NP_000264.2:p.Arg27=
Search 100 bp 5'
Search 100 bp 3'