Canonical Allele Identifier: CA2580102080

Gene: GPR143

Linked Data

• ClinVar Variation Id: 10525
• ClinVar RCV Id: RCV000011271 ; RCV002512969

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765577_9765595dup , CM000685.2:g.9765577_9765595dup	GRCh38
NC_000023.10:g.9733617_9733635dup , CM000685.1:g.9733617_9733635dup	GRCh37
NC_000023.9:g.9693617_9693635dup	NCBI36
NG_009074.1:g.5291_5309dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.231_249dup MANE Select	ENSP00000417161.1:p.Gly84ArgfsTer23
ENST00000431126.1:c.-3+533_-3+551dup	ENSP00000406138.1:n.-3+533_-3+551dup
ENST00000447366.5:c.-2-4761_-2-4743dup	ENSP00000390546.2:n.-2-4761_-2-4743dup
ENST00000467482.5:c.231_249dup	ENSP00000417161.1:p.Gly84ArgfsTer23
NM_000273.2:c.231_249dup	NP_000264.2:p.Gly84ArgfsTer23
XM_005274541.2:c.231_249dup	XP_005274598.1:p.Gly84ArgfsTer23
XM_005274541.3:c.231_249dup	XP_005274598.1:p.Gly84ArgfsTer23
XM_024452387.1:c.-2-4761_-2-4743dup	XP_024308155.1:n.-2-4761_-2-4743dup
XM_024452388.1:c.-2-4761_-2-4743dup	XP_024308156.1:n.-2-4761_-2-4743dup
NM_000273.3:c.231_249dup MANE Select	NP_000264.2:p.Gly84ArgfsTer23