Canonical Allele Identifier: CA2590950845

Gene: GPR143

Linked Data

• gnomAD v3: X-9765312-AGCAGGTCCCAACCCGCGGGCCTCAAGCCCTCAGCCGGGGACCGAGCAGGTCCCAACCAGCCAGCTACGCGCCCTCAGCCCTGCACCGG-A
• gnomAD v4: X-9765312-AGCAGGTCCCAACCCGCGGGCCTCAAGCCCTCAGCCGGGGACCGAGCAGGTCCCAACCAGCCAGCTACGCGCCCTCAGCCCTGCACCGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765319_9765406del , CM000685.2:g.9765319_9765406del	GRCh38
NC_000023.10:g.9733359_9733446del , CM000685.1:g.9733359_9733446del	GRCh37
NC_000023.9:g.9693359_9693446del	NCBI36
NG_009074.1:g.5478_5565del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+168_250+255del MANE Select	ENSP00000417161.1:n.250+168_250+255del
ENST00000431126.1:c.-3+720_-3+807del	ENSP00000406138.1:n.-3+720_-3+807del
ENST00000447366.5:c.-2-4574_-2-4487del	ENSP00000390546.2:n.-2-4574_-2-4487del
ENST00000467482.5:c.250+168_250+255del	ENSP00000417161.1:n.250+168_250+255del
NM_000273.2:c.250+168_250+255del	NP_000264.2:n.250+168_250+255del
XM_005274541.2:c.250+168_250+255del	XP_005274598.1:n.250+168_250+255del
XM_005274541.3:c.250+168_250+255del	XP_005274598.1:n.250+168_250+255del
XM_024452387.1:c.-2-4574_-2-4487del	XP_024308155.1:n.-2-4574_-2-4487del
XM_024452388.1:c.-2-4574_-2-4487del	XP_024308156.1:n.-2-4574_-2-4487del
NM_000273.3:c.250+168_250+255del MANE Select	NP_000264.2:n.250+168_250+255del