Canonical Allele Identifier: CA746833115

Gene: RSPO4

Linked Data

• dbSNP Id: rs1192127065
• MyVariant Identifiers: chr20:g.948970_948972del (hg19) ; chr20:g.968327_968329del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.968327_968329del , CM000682.2:g.968327_968329del	GRCh38
NC_000020.10:g.948970_948972del , CM000682.1:g.948970_948972del	GRCh37
NC_000020.9:g.896970_896972del	NCBI36
NG_013043.1:g.38936_38938del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.80-191_80-189del MANE Select	ENSP00000217260.4:n.80-191_80-189del
ENST00000217260.8:c.80-191_80-189del	ENSP00000217260.4:n.80-191_80-189del
ENST00000400634.2:c.80-191_80-189del	ENSP00000383475.2:n.80-191_80-189del
NM_001029871.3:c.80-191_80-189del	NP_001025042.2:n.80-191_80-189del
NM_001040007.2:c.80-191_80-189del	NP_001035096.1:n.80-191_80-189del
XM_011529232.1:c.128-191_128-189del	XP_011527534.1:n.128-191_128-189del
XM_011529233.1:c.128-191_128-189del	XP_011527535.1:n.128-191_128-189del
XR_937068.1:n.200-191_200-189del
XR_937069.1:n.195-191_195-189del
XM_017027839.1:c.80-191_80-189del	XP_016883328.1:n.80-191_80-189del
NM_001029871.4:c.80-191_80-189del MANE Select	NP_001025042.2:n.80-191_80-189del
NM_001040007.3:c.80-191_80-189del	NP_001035096.1:n.80-191_80-189del