Canonical Allele Identifier: CA2693067548

Gene: GPR143

Linked Data

• gnomAD v4: X-9765510-ACGCGCCCTCACCCAGGCGCTGATCAGATTCCAACCCGCGGGCCGCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765519_9765564del , CM000685.2:g.9765519_9765564del	GRCh38
NC_000023.10:g.9733559_9733604del , CM000685.1:g.9733559_9733604del	GRCh37
NC_000023.9:g.9693559_9693604del	NCBI36
NG_009074.1:g.5322_5367del

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.250+12_250+57del MANE Select	ENSP00000417161.1:n.250+12_250+57del
ENST00000431126.1:c.-3+564_-3+609del	ENSP00000406138.1:n.-3+564_-3+609del
ENST00000447366.5:c.-2-4730_-2-4685del	ENSP00000390546.2:n.-2-4730_-2-4685del
ENST00000467482.5:c.250+12_250+57del	ENSP00000417161.1:n.250+12_250+57del
NM_000273.2:c.250+12_250+57del	NP_000264.2:n.250+12_250+57del
XM_005274541.2:c.250+12_250+57del	XP_005274598.1:n.250+12_250+57del
XM_005274541.3:c.250+12_250+57del	XP_005274598.1:n.250+12_250+57del
XM_024452387.1:c.-2-4730_-2-4685del	XP_024308155.1:n.-2-4730_-2-4685del
XM_024452388.1:c.-2-4730_-2-4685del	XP_024308156.1:n.-2-4730_-2-4685del
NM_000273.3:c.250+12_250+57del MANE Select	NP_000264.2:n.250+12_250+57del