Canonical Allele Identifier: CA880114335

Gene: GPR143

Linked Data

• dbSNP Id: rs1193390673
• gnomAD v3: X-9765363-CCCAACCAGCCAGCTACGCGCCCTCAGCCCTGCACCGGGCAGGTT-C
• gnomAD v4: X-9765363-CCCAACCAGCCAGCTACGCGCCCTCAGCCCTGCACCGGGCAGGTT-C
• MyVariant Identifiers: chrX:g.9733404_9733447del (hg19) ; chrX:g.9765364_9765407del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765370_9765413del , CM000685.2:g.9765370_9765413del	GRCh38
NC_000023.10:g.9733410_9733453del , CM000685.1:g.9733410_9733453del	GRCh37
NC_000023.9:g.9693410_9693453del	NCBI36
NG_009074.1:g.5471_5514del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+161_250+204del MANE Select	ENSP00000417161.1:n.250+161_250+204del
ENST00000431126.1:c.-3+713_-3+756del	ENSP00000406138.1:n.-3+713_-3+756del
ENST00000447366.5:c.-2-4581_-2-4538del	ENSP00000390546.2:n.-2-4581_-2-4538del
ENST00000467482.5:c.250+161_250+204del	ENSP00000417161.1:n.250+161_250+204del
NM_000273.2:c.250+161_250+204del	NP_000264.2:n.250+161_250+204del
XM_005274541.2:c.250+161_250+204del	XP_005274598.1:n.250+161_250+204del
XM_005274541.3:c.250+161_250+204del	XP_005274598.1:n.250+161_250+204del
XM_024452387.1:c.-2-4581_-2-4538del	XP_024308155.1:n.-2-4581_-2-4538del
XM_024452388.1:c.-2-4581_-2-4538del	XP_024308156.1:n.-2-4581_-2-4538del
NM_000273.3:c.250+161_250+204del MANE Select	NP_000264.2:n.250+161_250+204del