Canonical Allele Identifier: CA2415032466

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765552_9765554delinsCCG , CM000685.2:g.9765552_9765554delinsCCG	GRCh38
NC_000023.10:g.9733592_9733594delinsCCG , CM000685.1:g.9733592_9733594delinsCCG	GRCh37
NC_000023.9:g.9693592_9693594delinsCCG	NCBI36
NG_009074.1:g.5324_5326delinsCGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.250+14_250+16delinsCGG MANE Select	ENSP00000417161.1:n.250+14_250+16delinsCG...
ENST00000431126.1:c.-3+566_-3+568delinsCGG	ENSP00000406138.1:n.-3+566_-3+568delinsCG...
ENST00000447366.5:c.-2-4728_-2-4726delinsCGG	ENSP00000390546.2:n.-2-4728_-2-4726delins...
ENST00000467482.5:c.250+14_250+16delinsCGG	ENSP00000417161.1:n.250+14_250+16delinsCG...
NM_000273.2:c.250+14_250+16delinsCGG	NP_000264.2:n.250+14_250+16delinsCGG
XM_005274541.2:c.250+14_250+16delinsCGG	XP_005274598.1:n.250+14_250+16delinsCGG
XM_005274541.3:c.250+14_250+16delinsCGG	XP_005274598.1:n.250+14_250+16delinsCGG
XM_024452387.1:c.-2-4728_-2-4726delinsCGG	XP_024308155.1:n.-2-4728_-2-4726delinsCGG...
XM_024452388.1:c.-2-4728_-2-4726delinsCGG	XP_024308156.1:n.-2-4728_-2-4726delinsCGG...
NM_000273.3:c.250+14_250+16delinsCGG MANE Select	NP_000264.2:n.250+14_250+16delinsCGG