Canonical Allele Identifier: CA640487416

Gene: GPR143

Linked Data

• dbSNP Id: rs1236718363
• gnomAD v2: X-9733197-C-T
• gnomAD v3: X-9765157-C-T
• gnomAD v4: X-9765157-C-T
• MyVariant Identifiers: chrX:g.9733197C>T (hg19) ; chrX:g.9765157C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765157C>T , CM000685.2:g.9765157C>T	GRCh38
NC_000023.10:g.9733197C>T , CM000685.1:g.9733197C>T	GRCh37
NC_000023.9:g.9693197C>T	NCBI36
NG_009074.1:g.5721G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+411G>A MANE Select	ENSP00000417161.1:n.250+411G>A
ENST00000431126.1:c.-3+963G>A	ENSP00000406138.1:n.-3+963G>A
ENST00000447366.5:c.-2-4331G>A	ENSP00000390546.2:n.-2-4331G>A
ENST00000467482.5:c.250+411G>A	ENSP00000417161.1:n.250+411G>A
NM_000273.2:c.250+411G>A	NP_000264.2:n.250+411G>A
XM_005274541.2:c.250+411G>A	XP_005274598.1:n.250+411G>A
XM_005274541.3:c.250+411G>A	XP_005274598.1:n.250+411G>A
XM_024452387.1:c.-2-4331G>A	XP_024308155.1:n.-2-4331G>A
XM_024452388.1:c.-2-4331G>A	XP_024308156.1:n.-2-4331G>A
NM_000273.3:c.250+411G>A MANE Select	NP_000264.2:n.250+411G>A