Canonical Allele Identifier: CA2345447556

Gene: RSPO4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967830_967832delinsAGT , CM000682.2:g.967830_967832delinsAGT	GRCh38
NC_000020.10:g.948473_948475delinsAGT , CM000682.1:g.948473_948475delinsAGT	GRCh37
NC_000020.9:g.896473_896475delinsAGT	NCBI36
NG_013043.1:g.39433_39435delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.268+118_268+120delinsACT MANE Select	ENSP00000217260.4:n.268+118_268+120delinsACT
ENST00000217260.8:c.268+118_268+120delinsACT	ENSP00000217260.4:n.268+118_268+120delinsACT
ENST00000400634.2:c.268+118_268+120delinsACT	ENSP00000383475.2:n.268+118_268+120delinsACT
NM_001029871.3:c.268+118_268+120delinsACT	NP_001025042.2:n.268+118_268+120delinsACT
NM_001040007.2:c.268+118_268+120delinsACT	NP_001035096.1:n.268+118_268+120delinsACT
XM_011529232.1:c.316+118_316+120delinsACT	XP_011527534.1:n.316+118_316+120delinsACT
XM_011529233.1:c.316+118_316+120delinsACT	XP_011527535.1:n.316+118_316+120delinsACT
XR_937068.1:n.388+118_388+120delinsACT
XR_937069.1:n.383+118_383+120delinsACT
XM_017027839.1:c.268+118_268+120delinsACT	XP_016883328.1:n.268+118_268+120delinsACT
NM_001029871.4:c.268+118_268+120delinsACT MANE Select	NP_001025042.2:n.268+118_268+120delinsACT
NM_001040007.3:c.268+118_268+120delinsACT	NP_001035096.1:n.268+118_268+120delinsACT