Canonical Allele Identifier: CA1014681998

Gene: RSPO4

Linked Data

• dbSNP Id: rs1984295441
• gnomAD v3: 20-968279-CCCTTA-C
• gnomAD v4: 20-968279-CCCTTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.968281_968285del , CM000682.2:g.968281_968285del	GRCh38
NC_000020.10:g.948924_948928del , CM000682.1:g.948924_948928del	GRCh37
NC_000020.9:g.896924_896928del	NCBI36
NG_013043.1:g.38981_38985del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.80-146_80-142del MANE Select	ENSP00000217260.4:n.80-146_80-142del
ENST00000217260.8:c.80-146_80-142del	ENSP00000217260.4:n.80-146_80-142del
ENST00000400634.2:c.80-146_80-142del	ENSP00000383475.2:n.80-146_80-142del
NM_001029871.3:c.80-146_80-142del	NP_001025042.2:n.80-146_80-142del
NM_001040007.2:c.80-146_80-142del	NP_001035096.1:n.80-146_80-142del
XM_011529232.1:c.128-146_128-142del	XP_011527534.1:n.128-146_128-142del
XM_011529233.1:c.128-146_128-142del	XP_011527535.1:n.128-146_128-142del
XR_937068.1:n.200-146_200-142del
XR_937069.1:n.195-146_195-142del
XM_017027839.1:c.80-146_80-142del	XP_016883328.1:n.80-146_80-142del
NM_001029871.4:c.80-146_80-142del MANE Select	NP_001025042.2:n.80-146_80-142del
NM_001040007.3:c.80-146_80-142del	NP_001035096.1:n.80-146_80-142del