Canonical Allele Identifier: CA2415032389

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765398C= , CM000685.2:g.9765398C=	GRCh38
NC_000023.10:g.9733438C= , CM000685.1:g.9733438C=	GRCh37
NC_000023.9:g.9693438C=	NCBI36
NG_009074.1:g.5480G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.250+170G= MANE Select	ENSP00000417161.1:n.250+170G=
ENST00000431126.1:c.-3+722G=	ENSP00000406138.1:n.-3+722G=
ENST00000447366.5:c.-2-4572G=	ENSP00000390546.2:n.-2-4572G=
ENST00000467482.5:c.250+170G=	ENSP00000417161.1:n.250+170G=
NM_000273.2:c.250+170G=	NP_000264.2:n.250+170G=
XM_005274541.2:c.250+170G=	XP_005274598.1:n.250+170G=
XM_005274541.3:c.250+170G=	XP_005274598.1:n.250+170G=
XM_024452387.1:c.-2-4572G=	XP_024308155.1:n.-2-4572G=
XM_024452388.1:c.-2-4572G=	XP_024308156.1:n.-2-4572G=
NM_000273.3:c.250+170G= MANE Select	NP_000264.2:n.250+170G=