Canonical Allele Identifier: CA2415032278

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765165_9765167delinsTTC , CM000685.2:g.9765165_9765167delinsTTC	GRCh38
NC_000023.10:g.9733205_9733207delinsTTC , CM000685.1:g.9733205_9733207delinsTTC	GRCh37
NC_000023.9:g.9693205_9693207delinsTTC	NCBI36
NG_009074.1:g.5711_5713delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+401_250+403delinsGAA MANE Select	ENSP00000417161.1:n.250+401_250+403delinsGAA
ENST00000431126.1:c.-3+953_-3+955delinsGAA	ENSP00000406138.1:n.-3+953_-3+955delinsGAA
ENST00000447366.5:c.-2-4341_-2-4339delinsGAA	ENSP00000390546.2:n.-2-4341_-2-4339delinsGAA
ENST00000467482.5:c.250+401_250+403delinsGAA	ENSP00000417161.1:n.250+401_250+403delinsGAA
NM_000273.2:c.250+401_250+403delinsGAA	NP_000264.2:n.250+401_250+403delinsGAA
XM_005274541.2:c.250+401_250+403delinsGAA	XP_005274598.1:n.250+401_250+403delinsGAA
XM_005274541.3:c.250+401_250+403delinsGAA	XP_005274598.1:n.250+401_250+403delinsGAA
XM_024452387.1:c.-2-4341_-2-4339delinsGAA	XP_024308155.1:n.-2-4341_-2-4339delinsGAA
XM_024452388.1:c.-2-4341_-2-4339delinsGAA	XP_024308156.1:n.-2-4341_-2-4339delinsGAA
NM_000273.3:c.250+401_250+403delinsGAA MANE Select	NP_000264.2:n.250+401_250+403delinsGAA