Canonical Allele Identifier: CA2651557602

Gene: RSPO4

Linked Data

• gnomAD v4: 20-967808-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967810del , CM000682.2:g.967810del	GRCh38
NC_000020.10:g.948453del , CM000682.1:g.948453del	GRCh37
NC_000020.9:g.896453del	NCBI36
NG_013043.1:g.39456del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.268+141del MANE Select	ENSP00000217260.4:n.268+141del
ENST00000217260.8:c.268+141del	ENSP00000217260.4:n.268+141del
ENST00000400634.2:c.268+141del	ENSP00000383475.2:n.268+141del
NM_001029871.3:c.268+141del	NP_001025042.2:n.268+141del
NM_001040007.2:c.268+141del	NP_001035096.1:n.268+141del
XM_011529232.1:c.316+141del	XP_011527534.1:n.316+141del
XM_011529233.1:c.316+141del	XP_011527535.1:n.316+141del
XR_937068.1:n.388+141del
XR_937069.1:n.383+141del
XM_017027839.1:c.268+141del	XP_016883328.1:n.268+141del
NM_001029871.4:c.268+141del MANE Select	NP_001025042.2:n.268+141del
NM_001040007.3:c.268+141del	NP_001035096.1:n.268+141del