Canonical Allele Identifier: CA2345447598

Gene: RSPO4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967878_967879delinsGA , CM000682.2:g.967878_967879delinsGA	GRCh38
NC_000020.10:g.948521_948522delinsGA , CM000682.1:g.948521_948522delinsGA	GRCh37
NC_000020.9:g.896521_896522delinsGA	NCBI36
NG_013043.1:g.39386_39387delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.268+71_268+72delinsTC MANE Select	ENSP00000217260.4:n.268+71_268+72delinsTC
ENST00000217260.8:c.268+71_268+72delinsTC	ENSP00000217260.4:n.268+71_268+72delinsTC
ENST00000400634.2:c.268+71_268+72delinsTC	ENSP00000383475.2:n.268+71_268+72delinsTC
NM_001029871.3:c.268+71_268+72delinsTC	NP_001025042.2:n.268+71_268+72delinsTC
NM_001040007.2:c.268+71_268+72delinsTC	NP_001035096.1:n.268+71_268+72delinsTC
XM_011529232.1:c.316+71_316+72delinsTC	XP_011527534.1:n.316+71_316+72delinsTC
XM_011529233.1:c.316+71_316+72delinsTC	XP_011527535.1:n.316+71_316+72delinsTC
XR_937068.1:n.388+71_388+72delinsTC
XR_937069.1:n.383+71_383+72delinsTC
XM_017027839.1:c.268+71_268+72delinsTC	XP_016883328.1:n.268+71_268+72delinsTC
NM_001029871.4:c.268+71_268+72delinsTC MANE Select	NP_001025042.2:n.268+71_268+72delinsTC
NM_001040007.3:c.268+71_268+72delinsTC	NP_001035096.1:n.268+71_268+72delinsTC