Canonical Allele Identifier: CA1130984035

Gene: GPR143

Linked Data

• gnomAD v3: X-9765156-CCGATCAAGTTCCAACCCGAGTGGATCGAGTTCCAACCTGCGGGCCATGCGCCCTCACCCGGGCAT-C
• gnomAD v4: X-9765156-CCGATCAAGTTCCAACCCGAGTGGATCGAGTTCCAACCTGCGGGCCATGCGCCCTCACCCGGGCAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765162_9765226del , CM000685.2:g.9765162_9765226del	GRCh38
NC_000023.10:g.9733202_9733266del , CM000685.1:g.9733202_9733266del	GRCh37
NC_000023.9:g.9693202_9693266del	NCBI36
NG_009074.1:g.5657_5721del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+347_250+411del MANE Select	ENSP00000417161.1:n.250+347_250+411del
ENST00000431126.1:c.-3+899_-3+963del	ENSP00000406138.1:n.-3+899_-3+963del
ENST00000447366.5:c.-2-4395_-2-4331del	ENSP00000390546.2:n.-2-4395_-2-4331del
ENST00000467482.5:c.250+347_250+411del	ENSP00000417161.1:n.250+347_250+411del
NM_000273.2:c.250+347_250+411del	NP_000264.2:n.250+347_250+411del
XM_005274541.2:c.250+347_250+411del	XP_005274598.1:n.250+347_250+411del
XM_005274541.3:c.250+347_250+411del	XP_005274598.1:n.250+347_250+411del
XM_024452387.1:c.-2-4395_-2-4331del	XP_024308155.1:n.-2-4395_-2-4331del
XM_024452388.1:c.-2-4395_-2-4331del	XP_024308156.1:n.-2-4395_-2-4331del
NM_000273.3:c.250+347_250+411del MANE Select	NP_000264.2:n.250+347_250+411del