Canonical Allele Identifier: CA326106967

Gene: GPR143

Linked Data

• dbSNP Id: rs57576405
• gnomAD v2: X-9733156-G-C
• gnomAD v3: X-9765116-G-C
• gnomAD v4: X-9765116-G-C
• MyVariant Identifiers: chrX:g.9733156G>C (hg19) ; chrX:g.9765116G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765116G>C , CM000685.2:g.9765116G>C	GRCh38
NC_000023.10:g.9733156G>C , CM000685.1:g.9733156G>C	GRCh37
NC_000023.9:g.9693156G>C	NCBI36
NG_009074.1:g.5762C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+452C>G MANE Select	ENSP00000417161.1:n.250+452C>G
ENST00000431126.1:c.-3+1004C>G	ENSP00000406138.1:n.-3+1004C>G
ENST00000447366.5:c.-2-4290C>G	ENSP00000390546.2:n.-2-4290C>G
ENST00000467482.5:c.250+452C>G	ENSP00000417161.1:n.250+452C>G
NM_000273.2:c.250+452C>G	NP_000264.2:n.250+452C>G
XM_005274541.2:c.250+452C>G	XP_005274598.1:n.250+452C>G
XM_005274541.3:c.250+452C>G	XP_005274598.1:n.250+452C>G
XM_024452387.1:c.-2-4290C>G	XP_024308155.1:n.-2-4290C>G
XM_024452388.1:c.-2-4290C>G	XP_024308156.1:n.-2-4290C>G
NM_000273.3:c.250+452C>G MANE Select	NP_000264.2:n.250+452C>G