Canonical Allele Identifier: CA2693067481

Gene: GPR143

Linked Data

• gnomAD v4: X-9765467-TGCGCCCTTATCCGGGCACCAGTCGGGTCTCAACCTGCGGGCCACGCGCCCTCACCCAGGCGCTGATCAGATTCCAACCCGCGGGCCGCGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765477_9765566del , CM000685.2:g.9765477_9765566del	GRCh38
NC_000023.10:g.9733517_9733606del , CM000685.1:g.9733517_9733606del	GRCh37
NC_000023.9:g.9693517_9693606del	NCBI36
NG_009074.1:g.5321_5410del

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.250+11_250+100del MANE Select	ENSP00000417161.1:n.250+11_250+100del
ENST00000431126.1:c.-3+563_-3+652del	ENSP00000406138.1:n.-3+563_-3+652del
ENST00000447366.5:c.-2-4731_-2-4642del	ENSP00000390546.2:n.-2-4731_-2-4642del
ENST00000467482.5:c.250+11_250+100del	ENSP00000417161.1:n.250+11_250+100del
NM_000273.2:c.250+11_250+100del	NP_000264.2:n.250+11_250+100del
XM_005274541.2:c.250+11_250+100del	XP_005274598.1:n.250+11_250+100del
XM_005274541.3:c.250+11_250+100del	XP_005274598.1:n.250+11_250+100del
XM_024452387.1:c.-2-4731_-2-4642del	XP_024308155.1:n.-2-4731_-2-4642del
XM_024452388.1:c.-2-4731_-2-4642del	XP_024308156.1:n.-2-4731_-2-4642del
NM_000273.3:c.250+11_250+100del MANE Select	NP_000264.2:n.250+11_250+100del