Canonical Allele Identifier: CA2415032375

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765351_9765377delinsGACCGAGCAGGTCCCAACCAGCCAGCT , CM000685.2:g.9765351_9765377delinsGACCGAGCAGGTCCCAACCAGCCAGCT	GRCh38
NC_000023.10:g.9733391_9733417delinsGACCGAGCAGGTCCCAACCAGCCAGCT , CM000685.1:g.9733391_9733417delinsGACCGAGCAGGTCCCAACCAGCCAGCT	GRCh37
NC_000023.9:g.9693391_9693417delinsGACCGAGCAGGTCCCAACCAGCCAGCT	NCBI36
NG_009074.1:g.5501_5527delinsAGCTGGCTGGTTGGGACCTGCTCGGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+191_250+217delinsAGCTGGCTGGTTGGGACCTGCTCGGTC MANE Select	ENSP00000417161.1:n.250+191_250+217delinsAGCTGGCTGGTTGGGACCTG...
ENST00000431126.1:c.-3+743_-3+769delinsAGCTGGCTGGTTGGGACCTGCTCGGTC	ENSP00000406138.1:n.-3+743_-3+769delinsAGCTGGCTGGTTGGGACCTGCT...
ENST00000447366.5:c.-2-4551_-2-4525delinsAGCTGGCTGGTTGGGACCTGCTCGGTC	ENSP00000390546.2:n.-2-4551_-2-4525delinsAGCTGGCTGGTTGGGACCTG...
ENST00000467482.5:c.250+191_250+217delinsAGCTGGCTGGTTGGGACCTGCTCGGTC	ENSP00000417161.1:n.250+191_250+217delinsAGCTGGCTGGTTGGGACCTG...
NM_000273.2:c.250+191_250+217delinsAGCTGGCTGGTTGGGACCTGCTCGGTC	NP_000264.2:n.250+191_250+217delinsAGCTGGCTGGTTGGGACCTGCTCGGT...
XM_005274541.2:c.250+191_250+217delinsAGCTGGCTGGTTGGGACCTGCTCGGTC	XP_005274598.1:n.250+191_250+217delinsAGCTGGCTGGTTGGGACCTGCTC...
XM_005274541.3:c.250+191_250+217delinsAGCTGGCTGGTTGGGACCTGCTCGGTC	XP_005274598.1:n.250+191_250+217delinsAGCTGGCTGGTTGGGACCTGCTC...
XM_024452387.1:c.-2-4551_-2-4525delinsAGCTGGCTGGTTGGGACCTGCTCGGTC	XP_024308155.1:n.-2-4551_-2-4525delinsAGCTGGCTGGTTGGGACCTGCTC...
XM_024452388.1:c.-2-4551_-2-4525delinsAGCTGGCTGGTTGGGACCTGCTCGGTC	XP_024308156.1:n.-2-4551_-2-4525delinsAGCTGGCTGGTTGGGACCTGCTC...
NM_000273.3:c.250+191_250+217delinsAGCTGGCTGGTTGGGACCTGCTCGGTC MANE Select	NP_000264.2:n.250+191_250+217delinsAGCTGGCTGGTTGGGACCTGCTCGGT...