Canonical Allele Identifier: CA2651558009

Gene: RSPO4

Linked Data

• gnomAD v4: 20-968251-CCAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.968256_968259del , CM000682.2:g.968256_968259del	GRCh38
NC_000020.10:g.948899_948902del , CM000682.1:g.948899_948902del	GRCh37
NC_000020.9:g.896899_896902del	NCBI36
NG_013043.1:g.39010_39013del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.80-117_80-114del MANE Select	ENSP00000217260.4:n.80-117_80-114del
ENST00000217260.8:c.80-117_80-114del	ENSP00000217260.4:n.80-117_80-114del
ENST00000400634.2:c.80-117_80-114del	ENSP00000383475.2:n.80-117_80-114del
NM_001029871.3:c.80-117_80-114del	NP_001025042.2:n.80-117_80-114del
NM_001040007.2:c.80-117_80-114del	NP_001035096.1:n.80-117_80-114del
XM_011529232.1:c.128-117_128-114del	XP_011527534.1:n.128-117_128-114del
XM_011529233.1:c.128-117_128-114del	XP_011527535.1:n.128-117_128-114del
XR_937068.1:n.200-117_200-114del
XR_937069.1:n.195-117_195-114del
XM_017027839.1:c.80-117_80-114del	XP_016883328.1:n.80-117_80-114del
NM_001029871.4:c.80-117_80-114del MANE Select	NP_001025042.2:n.80-117_80-114del
NM_001040007.3:c.80-117_80-114del	NP_001035096.1:n.80-117_80-114del