Canonical Allele Identifier: CA2345447547
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968102A= , CM000682.2:g.968102A= GRCh38
NC_000020.10:g.948745A= , CM000682.1:g.948745A= GRCh37
NC_000020.9:g.896745A= NCBI36
NG_013043.1:g.39163T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.116T= MANE Select ENSP00000217260.4:p.Ile39=
ENST00000217260.8:c.116T= ENSP00000217260.4:p.Ile39=
ENST00000400634.2:c.116T= ENSP00000383475.2:p.Ile39=
NM_001029871.3:c.116T= NP_001025042.2:p.Ile39=
NM_001040007.2:c.116T= NP_001035096.1:p.Ile39=
XM_011529232.1:c.164T= XP_011527534.1:p.Ile55=
XM_011529233.1:c.164T= XP_011527535.1:p.Ile55=
XR_937068.1:n.236T=
XR_937069.1:n.231T=
XM_017027839.1:c.116T= XP_016883328.1:p.Ile39=
NM_001029871.4:c.116T= MANE Select NP_001025042.2:p.Ile39=
NM_001040007.3:c.116T= NP_001035096.1:p.Ile39=