Canonical Allele Identifier: CA746832404

Gene: RSPO4

Linked Data

• dbSNP Id: rs1233774432
• gnomAD v3: 20-967801-GTCAGCCTGGACACAGGCAGGTATC-G
• gnomAD v4: 20-967801-GTCAGCCTGGACACAGGCAGGTATC-G
• MyVariant Identifiers: chr20:g.948445_948468del (hg19) ; chr20:g.967802_967825del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967806_967829del , CM000682.2:g.967806_967829del	GRCh38
NC_000020.10:g.948449_948472del , CM000682.1:g.948449_948472del	GRCh37
NC_000020.9:g.896449_896472del	NCBI36
NG_013043.1:g.39440_39463del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.268+125_268+148del MANE Select	ENSP00000217260.4:n.268+125_268+148del
ENST00000217260.8:c.268+125_268+148del	ENSP00000217260.4:n.268+125_268+148del
ENST00000400634.2:c.268+125_268+148del	ENSP00000383475.2:n.268+125_268+148del
NM_001029871.3:c.268+125_268+148del	NP_001025042.2:n.268+125_268+148del
NM_001040007.2:c.268+125_268+148del	NP_001035096.1:n.268+125_268+148del
XM_011529232.1:c.316+125_316+148del	XP_011527534.1:n.316+125_316+148del
XM_011529233.1:c.316+125_316+148del	XP_011527535.1:n.316+125_316+148del
XR_937068.1:n.388+125_388+148del
XR_937069.1:n.383+125_383+148del
XM_017027839.1:c.268+125_268+148del	XP_016883328.1:n.268+125_268+148del
NM_001029871.4:c.268+125_268+148del MANE Select	NP_001025042.2:n.268+125_268+148del
NM_001040007.3:c.268+125_268+148del	NP_001035096.1:n.268+125_268+148del