Canonical Allele Identifier: CA2819650387

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765559_9765560insACA , CM000685.2:g.9765559_9765560insACA	GRCh38
NC_000023.10:g.9733599_9733600insACA , CM000685.1:g.9733599_9733600insACA	GRCh37
NC_000023.9:g.9693599_9693600insACA	NCBI36
NG_009074.1:g.5318_5319insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+8_250+9insTGT MANE Select	ENSP00000417161.1:n.250+8_250+9insTGT
ENST00000431126.1:c.-3+560_-3+561insTGT	ENSP00000406138.1:n.-3+560_-3+561insTGT
ENST00000447366.5:c.-2-4734_-2-4733insTGT	ENSP00000390546.2:n.-2-4734_-2-4733insTGT
ENST00000467482.5:c.250+8_250+9insTGT	ENSP00000417161.1:n.250+8_250+9insTGT
NM_000273.2:c.250+8_250+9insTGT	NP_000264.2:n.250+8_250+9insTGT
XM_005274541.2:c.250+8_250+9insTGT	XP_005274598.1:n.250+8_250+9insTGT
XM_005274541.3:c.250+8_250+9insTGT	XP_005274598.1:n.250+8_250+9insTGT
XM_024452387.1:c.-2-4734_-2-4733insTGT	XP_024308155.1:n.-2-4734_-2-4733insTGT
XM_024452388.1:c.-2-4734_-2-4733insTGT	XP_024308156.1:n.-2-4734_-2-4733insTGT
NM_000273.3:c.250+8_250+9insTGT MANE Select	NP_000264.2:n.250+8_250+9insTGT