Canonical Allele Identifier: CA9725790

Gene: RSPO4

Linked Data

• dbSNP Id: rs748482022
• ExAC: 20:948817 G / GGA
• MyVariant Identifiers: chr20:g.948819_948820insGA (hg19) ; chr20:g.948817_948818insGA (hg19) ; chr20:g.968174_968175insGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.968183_968184dup , CM000682.2:g.968183_968184dup	GRCh38
NC_000020.10:g.948826_948827dup , CM000682.1:g.948826_948827dup	GRCh37
NC_000020.9:g.896826_896827dup	NCBI36
NG_013043.1:g.39089_39090dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.80-38_80-37dup MANE Select	ENSP00000217260.4:n.80-38_80-37dup
ENST00000217260.8:c.80-38_80-37dup	ENSP00000217260.4:n.80-38_80-37dup
ENST00000400634.2:c.80-38_80-37dup	ENSP00000383475.2:n.80-38_80-37dup
NM_001029871.3:c.80-38_80-37dup	NP_001025042.2:n.80-38_80-37dup
NM_001040007.2:c.80-38_80-37dup	NP_001035096.1:n.80-38_80-37dup
XM_011529232.1:c.128-38_128-37dup	XP_011527534.1:n.128-38_128-37dup
XM_011529233.1:c.128-38_128-37dup	XP_011527535.1:n.128-38_128-37dup
XR_937068.1:n.200-38_200-37dup
XR_937069.1:n.195-38_195-37dup
XM_017027839.1:c.80-38_80-37dup	XP_016883328.1:n.80-38_80-37dup
NM_001029871.4:c.80-38_80-37dup MANE Select	NP_001025042.2:n.80-38_80-37dup
NM_001040007.3:c.80-38_80-37dup	NP_001035096.1:n.80-38_80-37dup