Canonical Allele Identifier: CA2415032440

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765499A= , CM000685.2:g.9765499A=	GRCh38
NC_000023.10:g.9733539A= , CM000685.1:g.9733539A=	GRCh37
NC_000023.9:g.9693539A=	NCBI36
NG_009074.1:g.5379T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+69T= MANE Select	ENSP00000417161.1:n.250+69T=
ENST00000431126.1:c.-3+621T=	ENSP00000406138.1:n.-3+621T=
ENST00000447366.5:c.-2-4673T=	ENSP00000390546.2:n.-2-4673T=
ENST00000467482.5:c.250+69T=	ENSP00000417161.1:n.250+69T=
NM_000273.2:c.250+69T=	NP_000264.2:n.250+69T=
XM_005274541.2:c.250+69T=	XP_005274598.1:n.250+69T=
XM_005274541.3:c.250+69T=	XP_005274598.1:n.250+69T=
XM_024452387.1:c.-2-4673T=	XP_024308155.1:n.-2-4673T=
XM_024452388.1:c.-2-4673T=	XP_024308156.1:n.-2-4673T=
NM_000273.3:c.250+69T= MANE Select	NP_000264.2:n.250+69T=