Canonical Allele Identifier: CA2590950837

Gene: GPR143

Linked Data

• gnomAD v3: X-9765244-CCACGCA-C
• gnomAD v4: X-9765244-CCACGCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765246_9765251del , CM000685.2:g.9765246_9765251del	GRCh38
NC_000023.10:g.9733286_9733291del , CM000685.1:g.9733286_9733291del	GRCh37
NC_000023.9:g.9693286_9693291del	NCBI36
NG_009074.1:g.5628_5633del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+318_250+323del MANE Select	ENSP00000417161.1:n.250+318_250+323del
ENST00000431126.1:c.-3+870_-3+875del	ENSP00000406138.1:n.-3+870_-3+875del
ENST00000447366.5:c.-2-4424_-2-4419del	ENSP00000390546.2:n.-2-4424_-2-4419del
ENST00000467482.5:c.250+318_250+323del	ENSP00000417161.1:n.250+318_250+323del
NM_000273.2:c.250+318_250+323del	NP_000264.2:n.250+318_250+323del
XM_005274541.2:c.250+318_250+323del	XP_005274598.1:n.250+318_250+323del
XM_005274541.3:c.250+318_250+323del	XP_005274598.1:n.250+318_250+323del
XM_024452387.1:c.-2-4424_-2-4419del	XP_024308155.1:n.-2-4424_-2-4419del
XM_024452388.1:c.-2-4424_-2-4419del	XP_024308156.1:n.-2-4424_-2-4419del
NM_000273.3:c.250+318_250+323del MANE Select	NP_000264.2:n.250+318_250+323del