Canonical Allele Identifier: CA2345447509

Gene: RSPO4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967775_967776delinsCG , CM000682.2:g.967775_967776delinsCG	GRCh38
NC_000020.10:g.948418_948419delinsCG , CM000682.1:g.948418_948419delinsCG	GRCh37
NC_000020.9:g.896418_896419delinsCG	NCBI36
NG_013043.1:g.39489_39490delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.268+174_268+175delinsCG MANE Select	ENSP00000217260.4:n.268+174_268+175delinsCG
ENST00000217260.8:c.268+174_268+175delinsCG	ENSP00000217260.4:n.268+174_268+175delinsCG
ENST00000400634.2:c.268+174_268+175delinsCG	ENSP00000383475.2:n.268+174_268+175delinsCG
NM_001029871.3:c.268+174_268+175delinsCG	NP_001025042.2:n.268+174_268+175delinsCG
NM_001040007.2:c.268+174_268+175delinsCG	NP_001035096.1:n.268+174_268+175delinsCG
XM_011529232.1:c.316+174_316+175delinsCG	XP_011527534.1:n.316+174_316+175delinsCG
XM_011529233.1:c.316+174_316+175delinsCG	XP_011527535.1:n.316+174_316+175delinsCG
XR_937068.1:n.388+174_388+175delinsCG
XR_937069.1:n.383+174_383+175delinsCG
XM_017027839.1:c.268+174_268+175delinsCG	XP_016883328.1:n.268+174_268+175delinsCG
NM_001029871.4:c.268+174_268+175delinsCG MANE Select	NP_001025042.2:n.268+174_268+175delinsCG
NM_001040007.3:c.268+174_268+175delinsCG	NP_001035096.1:n.268+174_268+175delinsCG