Canonical Allele Identifier: CA2819650392

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765621_9765622insACA , CM000685.2:g.9765621_9765622insACA	GRCh38
NC_000023.10:g.9733661_9733662insACA , CM000685.1:g.9733661_9733662insACA	GRCh37
NC_000023.9:g.9693661_9693662insACA	NCBI36
NG_009074.1:g.5256_5257insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.196_197insTGT MANE Select	ENSP00000417161.1:p.Ala66delinsValSer
ENST00000431126.1:c.-3+498_-3+499insTGT	ENSP00000406138.1:n.-3+498_-3+499insTGT
ENST00000447366.5:c.-2-4796_-2-4795insTGT	ENSP00000390546.2:n.-2-4796_-2-4795insTGT
ENST00000467482.5:c.196_197insTGT	ENSP00000417161.1:p.Ala66delinsValSer
NM_000273.2:c.196_197insTGT	NP_000264.2:p.Ala66delinsValSer
XM_005274541.2:c.196_197insTGT	XP_005274598.1:p.Ala66delinsValSer
XM_005274541.3:c.196_197insTGT	XP_005274598.1:p.Ala66delinsValSer
XM_024452387.1:c.-2-4796_-2-4795insTGT	XP_024308155.1:n.-2-4796_-2-4795insTGT
XM_024452388.1:c.-2-4796_-2-4795insTGT	XP_024308156.1:n.-2-4796_-2-4795insTGT
NM_000273.3:c.196_197insTGT MANE Select	NP_000264.2:p.Ala66delinsValSer