Canonical Allele Identifier: CA2693067589

Gene: GPR143

Linked Data

• gnomAD v4: X-9765533-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765533T>G , CM000685.2:g.9765533T>G	GRCh38
NC_000023.10:g.9733573T>G , CM000685.1:g.9733573T>G	GRCh37
NC_000023.9:g.9693573T>G	NCBI36
NG_009074.1:g.5345A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+35A>C MANE Select	ENSP00000417161.1:n.250+35A>C
ENST00000431126.1:c.-3+587A>C	ENSP00000406138.1:n.-3+587A>C
ENST00000447366.5:c.-2-4707A>C	ENSP00000390546.2:n.-2-4707A>C
ENST00000467482.5:c.250+35A>C	ENSP00000417161.1:n.250+35A>C
NM_000273.2:c.250+35A>C	NP_000264.2:n.250+35A>C
XM_005274541.2:c.250+35A>C	XP_005274598.1:n.250+35A>C
XM_005274541.3:c.250+35A>C	XP_005274598.1:n.250+35A>C
XM_024452387.1:c.-2-4707A>C	XP_024308155.1:n.-2-4707A>C
XM_024452388.1:c.-2-4707A>C	XP_024308156.1:n.-2-4707A>C
NM_000273.3:c.250+35A>C MANE Select	NP_000264.2:n.250+35A>C