Canonical Allele Identifier: CA2514480463

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765333_9765334insGCGCGCGCCC , CM000685.2:g.9765333_9765334insGCGCGCGCCC	GRCh38
NC_000023.10:g.9733373_9733374insGCGCGCGCCC , CM000685.1:g.9733373_9733374insGCGCGCGCCC	GRCh37
NC_000023.9:g.9693373_9693374insGCGCGCGCCC	NCBI36
NG_009074.1:g.5546_5547insGCGCGCGCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+236_250+237insGCGCGCGCGG MANE Select	ENSP00000417161.1:n.250+236_250+237insGCGCGCGCGG
ENST00000431126.1:c.-3+788_-3+789insGCGCGCGCGG	ENSP00000406138.1:n.-3+788_-3+789insGCGCGCGCGG
ENST00000447366.5:c.-2-4506_-2-4505insGCGCGCGCGG	ENSP00000390546.2:n.-2-4506_-2-4505insGCGCGCGCGG
ENST00000467482.5:c.250+236_250+237insGCGCGCGCGG	ENSP00000417161.1:n.250+236_250+237insGCGCGCGCGG
NM_000273.2:c.250+236_250+237insGCGCGCGCGG	NP_000264.2:n.250+236_250+237insGCGCGCGCGG
XM_005274541.2:c.250+236_250+237insGCGCGCGCGG	XP_005274598.1:n.250+236_250+237insGCGCGCGCGG
XM_005274541.3:c.250+236_250+237insGCGCGCGCGG	XP_005274598.1:n.250+236_250+237insGCGCGCGCGG
XM_024452387.1:c.-2-4506_-2-4505insGCGCGCGCGG	XP_024308155.1:n.-2-4506_-2-4505insGCGCGCGCGG
XM_024452388.1:c.-2-4506_-2-4505insGCGCGCGCGG	XP_024308156.1:n.-2-4506_-2-4505insGCGCGCGCGG
NM_000273.3:c.250+236_250+237insGCGCGCGCGG MANE Select	NP_000264.2:n.250+236_250+237insGCGCGCGCGG