Canonical Allele Identifier: CA2693067530

Gene: GPR143

Linked Data

• gnomAD v4: X-9765502-TGCGGGCCACGCGCCCTCACCCAGGCGCTGATCAGATTCCAACCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765510_9765553del , CM000685.2:g.9765510_9765553del	GRCh38
NC_000023.10:g.9733550_9733593del , CM000685.1:g.9733550_9733593del	GRCh37
NC_000023.9:g.9693550_9693593del	NCBI36
NG_009074.1:g.5332_5375del

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.250+22_250+65del MANE Select	ENSP00000417161.1:n.250+22_250+65del
ENST00000431126.1:c.-3+574_-3+617del	ENSP00000406138.1:n.-3+574_-3+617del
ENST00000447366.5:c.-2-4720_-2-4677del	ENSP00000390546.2:n.-2-4720_-2-4677del
ENST00000467482.5:c.250+22_250+65del	ENSP00000417161.1:n.250+22_250+65del
NM_000273.2:c.250+22_250+65del	NP_000264.2:n.250+22_250+65del
XM_005274541.2:c.250+22_250+65del	XP_005274598.1:n.250+22_250+65del
XM_005274541.3:c.250+22_250+65del	XP_005274598.1:n.250+22_250+65del
XM_024452387.1:c.-2-4720_-2-4677del	XP_024308155.1:n.-2-4720_-2-4677del
XM_024452388.1:c.-2-4720_-2-4677del	XP_024308156.1:n.-2-4720_-2-4677del
NM_000273.3:c.250+22_250+65del MANE Select	NP_000264.2:n.250+22_250+65del