Canonical Allele Identifier: CA2345447740

Gene: RSPO4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.968336_968337delinsAG , CM000682.2:g.968336_968337delinsAG	GRCh38
NC_000020.10:g.948979_948980delinsAG , CM000682.1:g.948979_948980delinsAG	GRCh37
NC_000020.9:g.896979_896980delinsAG	NCBI36
NG_013043.1:g.38928_38929delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.80-199_80-198delinsCT MANE Select	ENSP00000217260.4:n.80-199_80-198delinsCT
ENST00000217260.8:c.80-199_80-198delinsCT	ENSP00000217260.4:n.80-199_80-198delinsCT
ENST00000400634.2:c.80-199_80-198delinsCT	ENSP00000383475.2:n.80-199_80-198delinsCT
NM_001029871.3:c.80-199_80-198delinsCT	NP_001025042.2:n.80-199_80-198delinsCT
NM_001040007.2:c.80-199_80-198delinsCT	NP_001035096.1:n.80-199_80-198delinsCT
XM_011529232.1:c.128-199_128-198delinsCT	XP_011527534.1:n.128-199_128-198delinsCT
XM_011529233.1:c.128-199_128-198delinsCT	XP_011527535.1:n.128-199_128-198delinsCT
XR_937068.1:n.200-199_200-198delinsCT
XR_937069.1:n.195-199_195-198delinsCT
XM_017027839.1:c.80-199_80-198delinsCT	XP_016883328.1:n.80-199_80-198delinsCT
NM_001029871.4:c.80-199_80-198delinsCT MANE Select	NP_001025042.2:n.80-199_80-198delinsCT
NM_001040007.3:c.80-199_80-198delinsCT	NP_001035096.1:n.80-199_80-198delinsCT