Canonical Allele Identifier: CA2415032544
Gene: GPR143 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765723A= , CM000685.2:g.9765723A= GRCh38
NC_000023.10:g.9733763A= , CM000685.1:g.9733763A= GRCh37
NC_000023.9:g.9693763A= NCBI36
NG_009074.1:g.5155T=

Transcript Alleles

HGVS Amino-acid change
ENST00000467482.6:c.95T= MANE Select ENSP00000417161.1:p.Leu32=
ENST00000431126.1:c.-3+397T= ENSP00000406138.1:n.-3+397T=
ENST00000447366.5:c.-2-4897T= ENSP00000390546.2:n.-2-4897T=
ENST00000467482.5:c.95T= ENSP00000417161.1:p.Leu32=
NM_000273.2:c.95T= NP_000264.2:p.Leu32=
XM_005274541.2:c.95T= XP_005274598.1:p.Leu32=
XM_005274541.3:c.95T= XP_005274598.1:p.Leu32=
XM_024452387.1:c.-2-4897T= XP_024308155.1:n.-2-4897T=
XM_024452388.1:c.-2-4897T= XP_024308156.1:n.-2-4897T=
NM_000273.3:c.95T= MANE Select NP_000264.2:p.Leu32=