Canonical Allele Identifier: CA1130984273

Gene: GPR143

Linked Data

• dbSNP Id: rs1431722100
• gnomAD v3: X-9765552-C-CCG
• gnomAD v4: X-9765552-C-CCG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765560_9765561dup , CM000685.2:g.9765560_9765561dup	GRCh38
NC_000023.10:g.9733600_9733601dup , CM000685.1:g.9733600_9733601dup	GRCh37
NC_000023.9:g.9693600_9693601dup	NCBI36
NG_009074.1:g.5324_5325dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000467482.6:c.250+14_250+15dup MANE Select	ENSP00000417161.1:n.250+14_250+15dup
ENST00000431126.1:c.-3+566_-3+567dup	ENSP00000406138.1:n.-3+566_-3+567dup
ENST00000447366.5:c.-2-4728_-2-4727dup	ENSP00000390546.2:n.-2-4728_-2-4727dup
ENST00000467482.5:c.250+14_250+15dup	ENSP00000417161.1:n.250+14_250+15dup
NM_000273.2:c.250+14_250+15dup	NP_000264.2:n.250+14_250+15dup
XM_005274541.2:c.250+14_250+15dup	XP_005274598.1:n.250+14_250+15dup
XM_005274541.3:c.250+14_250+15dup	XP_005274598.1:n.250+14_250+15dup
XM_024452387.1:c.-2-4728_-2-4727dup	XP_024308155.1:n.-2-4728_-2-4727dup
XM_024452388.1:c.-2-4728_-2-4727dup	XP_024308156.1:n.-2-4728_-2-4727dup
NM_000273.3:c.250+14_250+15dup MANE Select	NP_000264.2:n.250+14_250+15dup