Canonical Allele Identifier: CA515116102
Gene: GPR143 HGNC NCBI

Linked Data

gnomAD v4: X-9765617-C-T
MyVariant Identifiers: chrX:g.9733657C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765617C>T , CM000685.2:g.9765617C>T GRCh38
NC_000023.10:g.9733657C>T , CM000685.1:g.9733657C>T GRCh37
NC_000023.9:g.9693657C>T NCBI36
NG_009074.1:g.5261G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000467482.6:c.201G>A MANE Select ENSP00000417161.1:p.Ser67=
ENST00000431126.1:c.-3+503G>A ENSP00000406138.1:n.-3+503G>A
ENST00000447366.5:c.-2-4791G>A ENSP00000390546.2:n.-2-4791G>A
ENST00000467482.5:c.201G>A ENSP00000417161.1:p.Ser67=
NM_000273.2:c.201G>A NP_000264.2:p.Ser67=
XM_005274541.2:c.201G>A XP_005274598.1:p.Ser67=
XM_005274541.3:c.201G>A XP_005274598.1:p.Ser67=
XM_024452387.1:c.-2-4791G>A XP_024308155.1:n.-2-4791G>A
XM_024452388.1:c.-2-4791G>A XP_024308156.1:n.-2-4791G>A
NM_000273.3:c.201G>A MANE Select NP_000264.2:p.Ser67=