Canonical Allele Identifier: CA2693067621

Gene: GPR143

Linked Data

• gnomAD v4: X-9765554-G-GGCGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765554_9765555insGCGGC , CM000685.2:g.9765554_9765555insGCGGC	GRCh38
NC_000023.10:g.9733594_9733595insGCGGC , CM000685.1:g.9733594_9733595insGCGGC	GRCh37
NC_000023.9:g.9693594_9693595insGCGGC	NCBI36
NG_009074.1:g.5323_5324insGCCGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.250+13_250+14insGCCGC MANE Select	ENSP00000417161.1:n.250+13_250+14insGCCGC...
ENST00000431126.1:c.-3+565_-3+566insGCCGC	ENSP00000406138.1:n.-3+565_-3+566insGCCGC...
ENST00000447366.5:c.-2-4729_-2-4728insGCCGC	ENSP00000390546.2:n.-2-4729_-2-4728insGCC...
ENST00000467482.5:c.250+13_250+14insGCCGC	ENSP00000417161.1:n.250+13_250+14insGCCGC...
NM_000273.2:c.250+13_250+14insGCCGC	NP_000264.2:n.250+13_250+14insGCCGC
XM_005274541.2:c.250+13_250+14insGCCGC	XP_005274598.1:n.250+13_250+14insGCCGC
XM_005274541.3:c.250+13_250+14insGCCGC	XP_005274598.1:n.250+13_250+14insGCCGC
XM_024452387.1:c.-2-4729_-2-4728insGCCGC	XP_024308155.1:n.-2-4729_-2-4728insGCCGC
XM_024452388.1:c.-2-4729_-2-4728insGCCGC	XP_024308156.1:n.-2-4729_-2-4728insGCCGC
NM_000273.3:c.250+13_250+14insGCCGC MANE Select	NP_000264.2:n.250+13_250+14insGCCGC