Canonical Allele Identifier: CA515116203
Gene: GPR143 HGNC NCBI

Linked Data

gnomAD v4: X-9765722-G-T
MyVariant Identifiers: chrX:g.9733762G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765722G>T , CM000685.2:g.9765722G>T GRCh38
NC_000023.10:g.9733762G>T , CM000685.1:g.9733762G>T GRCh37
NC_000023.9:g.9693762G>T NCBI36
NG_009074.1:g.5156C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000467482.6:c.96C>A MANE Select ENSP00000417161.1:p.Leu32=
ENST00000431126.1:c.-3+398C>A ENSP00000406138.1:n.-3+398C>A
ENST00000447366.5:c.-2-4896C>A ENSP00000390546.2:n.-2-4896C>A
ENST00000467482.5:c.96C>A ENSP00000417161.1:p.Leu32=
NM_000273.2:c.96C>A NP_000264.2:p.Leu32=
XM_005274541.2:c.96C>A XP_005274598.1:p.Leu32=
XM_005274541.3:c.96C>A XP_005274598.1:p.Leu32=
XM_024452387.1:c.-2-4896C>A XP_024308155.1:n.-2-4896C>A
XM_024452388.1:c.-2-4896C>A XP_024308156.1:n.-2-4896C>A
NM_000273.3:c.96C>A MANE Select NP_000264.2:p.Leu32=