Canonical Allele Identifier: CA2415032462
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765548C= , CM000685.2:g.9765548C= GRCh38
NC_000023.10:g.9733588C= , CM000685.1:g.9733588C= GRCh37
NC_000023.9:g.9693588C= NCBI36
NG_009074.1:g.5330G=

Transcript Alleles

HGVS Amino-acid change
ENST00000467482.6:c.250+20G= MANE Select ENSP00000417161.1:n.250+20G=
ENST00000431126.1:c.-3+572G= ENSP00000406138.1:n.-3+572G=
ENST00000447366.5:c.-2-4722G= ENSP00000390546.2:n.-2-4722G=
ENST00000467482.5:c.250+20G= ENSP00000417161.1:n.250+20G=
NM_000273.2:c.250+20G= NP_000264.2:n.250+20G=
XM_005274541.2:c.250+20G= XP_005274598.1:n.250+20G=
XM_005274541.3:c.250+20G= XP_005274598.1:n.250+20G=
XM_024452387.1:c.-2-4722G= XP_024308155.1:n.-2-4722G=
XM_024452388.1:c.-2-4722G= XP_024308156.1:n.-2-4722G=
NM_000273.3:c.250+20G= MANE Select NP_000264.2:n.250+20G=