Canonical Allele Identifier: CA2415032479
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765572G= , CM000685.2:g.9765572G= GRCh38
NC_000023.10:g.9733612G= , CM000685.1:g.9733612G= GRCh37
NC_000023.9:g.9693612G= NCBI36
NG_009074.1:g.5306C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000467482.6:c.246C= MANE Select ENSP00000417161.1:p.Cys82=
ENST00000431126.1:c.-3+548C= ENSP00000406138.1:n.-3+548C=
ENST00000447366.5:c.-2-4746C= ENSP00000390546.2:n.-2-4746C=
ENST00000467482.5:c.246C= ENSP00000417161.1:p.Cys82=
NM_000273.2:c.246C= NP_000264.2:p.Cys82=
XM_005274541.2:c.246C= XP_005274598.1:p.Cys82=
XM_005274541.3:c.246C= XP_005274598.1:p.Cys82=
XM_024452387.1:c.-2-4746C= XP_024308155.1:n.-2-4746C=
XM_024452388.1:c.-2-4746C= XP_024308156.1:n.-2-4746C=
NM_000273.3:c.246C= MANE Select NP_000264.2:p.Cys82=