Canonical Allele Identifier: CA2693067542

Gene: GPR143

Linked Data

• gnomAD v4: X-9765508-CCACGCGCCCTCACCCAGGCGCTGATCAGATTCCAACCCGCGGGCCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765510_9765555del , CM000685.2:g.9765510_9765555del	GRCh38
NC_000023.10:g.9733550_9733595del , CM000685.1:g.9733550_9733595del	GRCh37
NC_000023.9:g.9693550_9693595del	NCBI36
NG_009074.1:g.5324_5369del

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.250+14_250+59del MANE Select	ENSP00000417161.1:n.250+14_250+59del
ENST00000431126.1:c.-3+566_-3+611del	ENSP00000406138.1:n.-3+566_-3+611del
ENST00000447366.5:c.-2-4728_-2-4683del	ENSP00000390546.2:n.-2-4728_-2-4683del
ENST00000467482.5:c.250+14_250+59del	ENSP00000417161.1:n.250+14_250+59del
NM_000273.2:c.250+14_250+59del	NP_000264.2:n.250+14_250+59del
XM_005274541.2:c.250+14_250+59del	XP_005274598.1:n.250+14_250+59del
XM_005274541.3:c.250+14_250+59del	XP_005274598.1:n.250+14_250+59del
XM_024452387.1:c.-2-4728_-2-4683del	XP_024308155.1:n.-2-4728_-2-4683del
XM_024452388.1:c.-2-4728_-2-4683del	XP_024308156.1:n.-2-4728_-2-4683del
NM_000273.3:c.250+14_250+59del MANE Select	NP_000264.2:n.250+14_250+59del