Canonical Allele Identifier: CA515116197
Gene: GPR143 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.9733756C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.9765716C>G , CM000685.2:g.9765716C>G GRCh38
NC_000023.10:g.9733756C>G , CM000685.1:g.9733756C>G GRCh37
NC_000023.9:g.9693756C>G NCBI36
NG_009074.1:g.5162G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000467482.6:c.102G>C MANE Select ENSP00000417161.1:p.Leu34=
ENST00000431126.1:c.-3+404G>C ENSP00000406138.1:n.-3+404G>C
ENST00000447366.5:c.-2-4890G>C ENSP00000390546.2:n.-2-4890G>C
ENST00000467482.5:c.102G>C ENSP00000417161.1:p.Leu34=
NM_000273.2:c.102G>C NP_000264.2:p.Leu34=
XM_005274541.2:c.102G>C XP_005274598.1:p.Leu34=
XM_005274541.3:c.102G>C XP_005274598.1:p.Leu34=
XM_024452387.1:c.-2-4890G>C XP_024308155.1:n.-2-4890G>C
XM_024452388.1:c.-2-4890G>C XP_024308156.1:n.-2-4890G>C
NM_000273.3:c.102G>C MANE Select NP_000264.2:p.Leu34=