Canonical Allele Identifier: CA640487423

Gene: GPR143

Linked Data

• gnomAD v2: X-9733259-C-CGCTG
• gnomAD v3: X-9765219-C-CGCTG
• gnomAD v4: X-9765219-C-CGCTG
• MyVariant Identifiers: chrX:g.9733259_9733260insGCTG (hg19) ; chrX:g.9765219_9765220insGCTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765219_9765220insGCTG , CM000685.2:g.9765219_9765220insGCTG	GRCh38
NC_000023.10:g.9733259_9733260insGCTG , CM000685.1:g.9733259_9733260insGCTG	GRCh37
NC_000023.9:g.9693259_9693260insGCTG	NCBI36
NG_009074.1:g.5658_5659insCAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+348_250+349insCAGC MANE Select	ENSP00000417161.1:n.250+348_250+349insCAGC
ENST00000431126.1:c.-3+900_-3+901insCAGC	ENSP00000406138.1:n.-3+900_-3+901insCAGC
ENST00000447366.5:c.-2-4394_-2-4393insCAGC	ENSP00000390546.2:n.-2-4394_-2-4393insCAGC
ENST00000467482.5:c.250+348_250+349insCAGC	ENSP00000417161.1:n.250+348_250+349insCAGC
NM_000273.2:c.250+348_250+349insCAGC	NP_000264.2:n.250+348_250+349insCAGC
XM_005274541.2:c.250+348_250+349insCAGC	XP_005274598.1:n.250+348_250+349insCAGC
XM_005274541.3:c.250+348_250+349insCAGC	XP_005274598.1:n.250+348_250+349insCAGC
XM_024452387.1:c.-2-4394_-2-4393insCAGC	XP_024308155.1:n.-2-4394_-2-4393insCAGC
XM_024452388.1:c.-2-4394_-2-4393insCAGC	XP_024308156.1:n.-2-4394_-2-4393insCAGC
NM_000273.3:c.250+348_250+349insCAGC MANE Select	NP_000264.2:n.250+348_250+349insCAGC