Canonical Allele Identifier: CA2693067512

Gene: GPR143

Linked Data

• gnomAD v4: X-9765490-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.9765490C>G , CM000685.2:g.9765490C>G	GRCh38
NC_000023.10:g.9733530C>G , CM000685.1:g.9733530C>G	GRCh37
NC_000023.9:g.9693530C>G	NCBI36
NG_009074.1:g.5388G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000467482.6:c.250+78G>C MANE Select	ENSP00000417161.1:n.250+78G>C
ENST00000431126.1:c.-3+630G>C	ENSP00000406138.1:n.-3+630G>C
ENST00000447366.5:c.-2-4664G>C	ENSP00000390546.2:n.-2-4664G>C
ENST00000467482.5:c.250+78G>C	ENSP00000417161.1:n.250+78G>C
NM_000273.2:c.250+78G>C	NP_000264.2:n.250+78G>C
XM_005274541.2:c.250+78G>C	XP_005274598.1:n.250+78G>C
XM_005274541.3:c.250+78G>C	XP_005274598.1:n.250+78G>C
XM_024452387.1:c.-2-4664G>C	XP_024308155.1:n.-2-4664G>C
XM_024452388.1:c.-2-4664G>C	XP_024308156.1:n.-2-4664G>C
NM_000273.3:c.250+78G>C MANE Select	NP_000264.2:n.250+78G>C