Canonical Allele Identifier: CA226184

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9759343_9759344insCGATCTC , CM000685.2:g.9759343_9759344insCGATCTC	GRCh38
NC_000023.10:g.9727383_9727384insCGATCTC , CM000685.1:g.9727383_9727384insCGATCTC	GRCh37
NC_000023.9:g.9687383_9687384insCGATCTC	NCBI36
NG_009074.1:g.11535_11536insAGATCGG

Transcript Alleles

HGVS	Amino-acid Change
NM_000273.3:c.444_445insAGATCGG MANE Select	NP_000264.2:p.Ala149ArgfsTer?
ENST00000467482.6:c.444_445insAGATCGG MANE Select	ENSP00000417161.1:p.Ala149ArgfsTer?
NM_000273.2:c.444_445insAGATCGG	NP_000264.2:p.Ala149ArgfsTer?
ENST00000431126.1:c.192_193insAGATCGG	ENSP00000406138.1:p.Ala65ArgfsTer?
ENST00000447366.5:c.192_193insAGATCGG	ENSP00000390546.2:p.Ala65ArgfsTer?
ENST00000467482.5:c.444_445insAGATCGG	ENSP00000417161.1:p.Ala149ArgfsTer?
ENST00000480178.1:n.52_53insAGATCGG
XM_005274541.2:c.444_445insAGATCGG	XP_005274598.1:p.Ala149ArgfsTer?
XM_005274541.3:c.444_445insAGATCGG	XP_005274598.1:p.Ala149ArgfsTer?
XM_024452387.1:c.192_193insAGATCGG	XP_024308155.1:p.Ala65ArgfsTer?
XM_024452388.1:c.192_193insAGATCGG	XP_024308156.1:p.Ala65ArgfsTer?