Canonical Allele Identifier: CA407970186

Gene: RSPO4

Linked Data

• COSMIC: COSM1029383
• MyVariant Identifiers: chr20:g.948601C>A (hg19) ; chr20:g.967958C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967958C>A , CM000682.2:g.967958C>A	GRCh38
NC_000020.10:g.948601C>A , CM000682.1:g.948601C>A	GRCh37
NC_000020.9:g.896601C>A	NCBI36
NG_013043.1:g.39307G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.260G>T MANE Select	ENSP00000217260.4:p.Arg87Met
ENST00000217260.8:c.260G>T	ENSP00000217260.4:p.Arg87Met
ENST00000400634.2:c.260G>T	ENSP00000383475.2:p.Arg87Met
NM_001029871.3:c.260G>T	NP_001025042.2:p.Arg87Met
NM_001040007.2:c.260G>T	NP_001035096.1:p.Arg87Met
XM_011529232.1:c.308G>T	XP_011527534.1:p.Arg103Met
XM_011529233.1:c.308G>T	XP_011527535.1:p.Arg103Met
XR_937068.1:n.380G>T
XR_937069.1:n.375G>T
XM_017027839.1:c.260G>T	XP_016883328.1:p.Arg87Met
NM_001029871.4:c.260G>T MANE Select	NP_001025042.2:p.Arg87Met
NM_001040007.3:c.260G>T	NP_001035096.1:p.Arg87Met