Canonical Allele Identifier: CA2415025113

Gene: GPR143

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9743637G= , CM000685.2:g.9743637G=	GRCh38
NC_000023.10:g.9711677G= , CM000685.1:g.9711677G=	GRCh37
NC_000023.9:g.9671677G=	NCBI36
NG_009074.1:g.27241C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.695C= MANE Select	ENSP00000417161.1:p.Thr232=
ENST00000431126.1:c.443C=	ENSP00000406138.1:p.Thr148=
ENST00000447366.5:c.443C=	ENSP00000390546.2:p.Thr148=
ENST00000467482.5:c.695C=	ENSP00000417161.1:p.Thr232=
NM_000273.2:c.695C=	NP_000264.2:p.Thr232=
XM_005274541.2:c.695C=	XP_005274598.1:p.Thr232=
XM_005274541.3:c.695C=	XP_005274598.1:p.Thr232=
XM_024452387.1:c.443C=	XP_024308155.1:p.Thr148=
XM_024452388.1:c.443C=	XP_024308156.1:p.Thr148=
NM_000273.3:c.695C= MANE Select	NP_000264.2:p.Thr232=