Canonical Allele Identifier: CA2815014437

Gene: RSPO4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967830_967831del , CM000682.2:g.967830_967831del	GRCh38
NC_000020.10:g.948473_948474del , CM000682.1:g.948473_948474del	GRCh37
NC_000020.9:g.896473_896474del	NCBI36
NG_013043.1:g.39436_39437del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.268+121_268+122del MANE Select	ENSP00000217260.4:n.268+121_268+122del
ENST00000217260.8:c.268+121_268+122del	ENSP00000217260.4:n.268+121_268+122del
ENST00000400634.2:c.268+121_268+122del	ENSP00000383475.2:n.268+121_268+122del
NM_001029871.3:c.268+121_268+122del	NP_001025042.2:n.268+121_268+122del
NM_001040007.2:c.268+121_268+122del	NP_001035096.1:n.268+121_268+122del
XM_011529232.1:c.316+121_316+122del	XP_011527534.1:n.316+121_316+122del
XM_011529233.1:c.316+121_316+122del	XP_011527535.1:n.316+121_316+122del
XR_937068.1:n.388+121_388+122del
XR_937069.1:n.383+121_383+122del
XM_017027839.1:c.268+121_268+122del	XP_016883328.1:n.268+121_268+122del
NM_001029871.4:c.268+121_268+122del MANE Select	NP_001025042.2:n.268+121_268+122del
NM_001040007.3:c.268+121_268+122del	NP_001035096.1:n.268+121_268+122del