Canonical Allele Identifier: CA326107050

Gene: GPR143

Linked Data

• dbSNP Id: rs771498174
• gnomAD v3: X-9765258-C-CCGGG
• gnomAD v4: X-9765258-C-CCGGG
• MyVariant Identifiers: chrX:g.9733298_9733299insCGGG (hg19) ; chrX:g.9765258_9765259insCGGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765259_9765262dup , CM000685.2:g.9765259_9765262dup	GRCh38
NC_000023.10:g.9733299_9733302dup , CM000685.1:g.9733299_9733302dup	GRCh37
NC_000023.9:g.9693299_9693302dup	NCBI36
NG_009074.1:g.5616_5619dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+306_250+309dup MANE Select	ENSP00000417161.1:n.250+306_250+309dup
ENST00000431126.1:c.-3+858_-3+861dup	ENSP00000406138.1:n.-3+858_-3+861dup
ENST00000447366.5:c.-2-4436_-2-4433dup	ENSP00000390546.2:n.-2-4436_-2-4433dup
ENST00000467482.5:c.250+306_250+309dup	ENSP00000417161.1:n.250+306_250+309dup
NM_000273.2:c.250+306_250+309dup	NP_000264.2:n.250+306_250+309dup
XM_005274541.2:c.250+306_250+309dup	XP_005274598.1:n.250+306_250+309dup
XM_005274541.3:c.250+306_250+309dup	XP_005274598.1:n.250+306_250+309dup
XM_024452387.1:c.-2-4436_-2-4433dup	XP_024308155.1:n.-2-4436_-2-4433dup
XM_024452388.1:c.-2-4436_-2-4433dup	XP_024308156.1:n.-2-4436_-2-4433dup
NM_000273.3:c.250+306_250+309dup MANE Select	NP_000264.2:n.250+306_250+309dup