Canonical Allele Identifier: CA2651557668

Gene: RSPO4

Linked Data

• gnomAD v4: 20-967851-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967851C>A , CM000682.2:g.967851C>A	GRCh38
NC_000020.10:g.948494C>A , CM000682.1:g.948494C>A	GRCh37
NC_000020.9:g.896494C>A	NCBI36
NG_013043.1:g.39414G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.268+99G>T MANE Select	ENSP00000217260.4:n.268+99G>T
ENST00000217260.8:c.268+99G>T	ENSP00000217260.4:n.268+99G>T
ENST00000400634.2:c.268+99G>T	ENSP00000383475.2:n.268+99G>T
NM_001029871.3:c.268+99G>T	NP_001025042.2:n.268+99G>T
NM_001040007.2:c.268+99G>T	NP_001035096.1:n.268+99G>T
XM_011529232.1:c.316+99G>T	XP_011527534.1:n.316+99G>T
XM_011529233.1:c.316+99G>T	XP_011527535.1:n.316+99G>T
XR_937068.1:n.388+99G>T
XR_937069.1:n.383+99G>T
XM_017027839.1:c.268+99G>T	XP_016883328.1:n.268+99G>T
NM_001029871.4:c.268+99G>T MANE Select	NP_001025042.2:n.268+99G>T
NM_001040007.3:c.268+99G>T	NP_001035096.1:n.268+99G>T