Canonical Allele Identifier: CA2345447691

Gene: RSPO4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.968279_968284delinsCCCTTA , CM000682.2:g.968279_968284delinsCCCTTA	GRCh38
NC_000020.10:g.948922_948927delinsCCCTTA , CM000682.1:g.948922_948927delinsCCCTTA	GRCh37
NC_000020.9:g.896922_896927delinsCCCTTA	NCBI36
NG_013043.1:g.38981_38986delinsTAAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.80-146_80-141delinsTAAGGG MANE Select	ENSP00000217260.4:n.80-146_80-141delinsTAAGGG
ENST00000217260.8:c.80-146_80-141delinsTAAGGG	ENSP00000217260.4:n.80-146_80-141delinsTAAGGG
ENST00000400634.2:c.80-146_80-141delinsTAAGGG	ENSP00000383475.2:n.80-146_80-141delinsTAAGGG
NM_001029871.3:c.80-146_80-141delinsTAAGGG	NP_001025042.2:n.80-146_80-141delinsTAAGGG
NM_001040007.2:c.80-146_80-141delinsTAAGGG	NP_001035096.1:n.80-146_80-141delinsTAAGGG
XM_011529232.1:c.128-146_128-141delinsTAAGGG	XP_011527534.1:n.128-146_128-141delinsTAAGGG
XM_011529233.1:c.128-146_128-141delinsTAAGGG	XP_011527535.1:n.128-146_128-141delinsTAAGGG
XR_937068.1:n.200-146_200-141delinsTAAGGG
XR_937069.1:n.195-146_195-141delinsTAAGGG
XM_017027839.1:c.80-146_80-141delinsTAAGGG	XP_016883328.1:n.80-146_80-141delinsTAAGGG
NM_001029871.4:c.80-146_80-141delinsTAAGGG MANE Select	NP_001025042.2:n.80-146_80-141delinsTAAGGG
NM_001040007.3:c.80-146_80-141delinsTAAGGG	NP_001035096.1:n.80-146_80-141delinsTAAGGG