Canonical Allele Identifier: CA226181

Gene: GPR143

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9759390A>G , CM000685.2:g.9759390A>G	GRCh38
NC_000023.10:g.9727430A>G , CM000685.1:g.9727430A>G	GRCh37
NC_000023.9:g.9687430A>G	NCBI36
NG_009074.1:g.11488T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.397T>C MANE Select	ENSP00000417161.1:p.Trp133Arg
ENST00000431126.1:c.145T>C	ENSP00000406138.1:p.Trp49Arg
ENST00000447366.5:c.145T>C	ENSP00000390546.2:p.Trp49Arg
ENST00000467482.5:c.397T>C	ENSP00000417161.1:p.Trp133Arg
ENST00000480178.1:n.5T>C
NM_000273.2:c.397T>C	NP_000264.2:p.Trp133Arg
XM_005274541.2:c.397T>C	XP_005274598.1:p.Trp133Arg
XM_005274541.3:c.397T>C	XP_005274598.1:p.Trp133Arg
XM_024452387.1:c.145T>C	XP_024308155.1:p.Trp49Arg
XM_024452388.1:c.145T>C	XP_024308156.1:p.Trp49Arg
NM_000273.3:c.397T>C MANE Select	NP_000264.2:p.Trp133Arg