Canonical Allele Identifier: CA412000827

Gene: GPR143

Linked Data

• gnomAD v4: X-9765738-C-A
• MyVariant Identifiers: chrX:g.9733778C>A (hg19) ; chrX:g.9765738C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765738C>A , CM000685.2:g.9765738C>A	GRCh38
NC_000023.10:g.9733778C>A , CM000685.1:g.9733778C>A	GRCh37
NC_000023.9:g.9693778C>A	NCBI36
NG_009074.1:g.5140G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.80G>T MANE Select	ENSP00000417161.1:p.Arg27Leu
ENST00000431126.1:c.-3+382G>T	ENSP00000406138.1:n.-3+382G>T
ENST00000447366.5:c.-2-4912G>T	ENSP00000390546.2:n.-2-4912G>T
ENST00000467482.5:c.80G>T	ENSP00000417161.1:p.Arg27Leu
NM_000273.2:c.80G>T	NP_000264.2:p.Arg27Leu
XM_005274541.2:c.80G>T	XP_005274598.1:p.Arg27Leu
XM_005274541.3:c.80G>T	XP_005274598.1:p.Arg27Leu
XM_024452387.1:c.-2-4912G>T	XP_024308155.1:n.-2-4912G>T
XM_024452388.1:c.-2-4912G>T	XP_024308156.1:n.-2-4912G>T
NM_000273.3:c.80G>T MANE Select	NP_000264.2:p.Arg27Leu