Canonical Allele Identifier: CA2577315598

Gene: RSPO4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967916_967917del , CM000682.2:g.967916_967917del	GRCh38
NC_000020.10:g.948559_948560del , CM000682.1:g.948559_948560del	GRCh37
NC_000020.9:g.896559_896560del	NCBI36
NG_013043.1:g.39348_39349del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.268+33_268+34del MANE Select	ENSP00000217260.4:n.268+33_268+34del
ENST00000217260.8:c.268+33_268+34del	ENSP00000217260.4:n.268+33_268+34del
ENST00000400634.2:c.268+33_268+34del	ENSP00000383475.2:n.268+33_268+34del
NM_001029871.3:c.268+33_268+34del	NP_001025042.2:n.268+33_268+34del
NM_001040007.2:c.268+33_268+34del	NP_001035096.1:n.268+33_268+34del
XM_011529232.1:c.316+33_316+34del	XP_011527534.1:n.316+33_316+34del
XM_011529233.1:c.316+33_316+34del	XP_011527535.1:n.316+33_316+34del
XR_937068.1:n.388+33_388+34del
XR_937069.1:n.383+33_383+34del
XM_017027839.1:c.268+33_268+34del	XP_016883328.1:n.268+33_268+34del
NM_001029871.4:c.268+33_268+34del MANE Select	NP_001025042.2:n.268+33_268+34del
NM_001040007.3:c.268+33_268+34del	NP_001035096.1:n.268+33_268+34del