Canonical Allele Identifier: CA2345447558
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968107G= , CM000682.2:g.968107G= GRCh38
NC_000020.10:g.948750G= , CM000682.1:g.948750G= GRCh37
NC_000020.9:g.896750G= NCBI36
NG_013043.1:g.39158C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.111C= MANE Select ENSP00000217260.4:p.Gly37=
ENST00000217260.8:c.111C= ENSP00000217260.4:p.Gly37=
ENST00000400634.2:c.111C= ENSP00000383475.2:p.Gly37=
NM_001029871.3:c.111C= NP_001025042.2:p.Gly37=
NM_001040007.2:c.111C= NP_001035096.1:p.Gly37=
XM_011529232.1:c.159C= XP_011527534.1:p.Gly53=
XM_011529233.1:c.159C= XP_011527535.1:p.Gly53=
XR_937068.1:n.231C=
XR_937069.1:n.226C=
XM_017027839.1:c.111C= XP_016883328.1:p.Gly37=
NM_001029871.4:c.111C= MANE Select NP_001025042.2:p.Gly37=
NM_001040007.3:c.111C= NP_001035096.1:p.Gly37=