Canonical Allele Identifier: CA2693067645

Gene: GPR143

Linked Data

• gnomAD v4: X-9765589-AGGCAGCGGCAGCGCGCAGGATGCGGACCGAGGCCGGCGGGGACGTCGCGGGGGACCCGGGGCCCGCGGGCCGGCGGCCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765596_9765674del , CM000685.2:g.9765596_9765674del	GRCh38
NC_000023.10:g.9733636_9733714del , CM000685.1:g.9733636_9733714del	GRCh37
NC_000023.9:g.9693636_9693714del	NCBI36
NG_009074.1:g.5210_5288del

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.150_228del MANE Select	ENSP00000417161.1:p.Gly51AlafsTer10
ENST00000431126.1:c.-3+452_-3+530del	ENSP00000406138.1:n.-3+452_-3+530del
ENST00000447366.5:c.-2-4842_-2-4764del	ENSP00000390546.2:n.-2-4842_-2-4764del
ENST00000467482.5:c.150_228del	ENSP00000417161.1:p.Gly51AlafsTer10
NM_000273.2:c.150_228del	NP_000264.2:p.Gly51AlafsTer10
XM_005274541.2:c.150_228del	XP_005274598.1:p.Gly51AlafsTer10
XM_005274541.3:c.150_228del	XP_005274598.1:p.Gly51AlafsTer10
XM_024452387.1:c.-2-4842_-2-4764del	XP_024308155.1:n.-2-4842_-2-4764del
XM_024452388.1:c.-2-4842_-2-4764del	XP_024308156.1:n.-2-4842_-2-4764del
NM_000273.3:c.150_228del MANE Select	NP_000264.2:p.Gly51AlafsTer10