Canonical Allele Identifier: CA515116201
Gene: GPR143 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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