Canonical Allele Identifier: CA2345447500
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968077A= , CM000682.2:g.968077A= GRCh38
NC_000020.10:g.948720A= , CM000682.1:g.948720A= GRCh37
NC_000020.9:g.896720A= NCBI36
NG_013043.1:g.39188T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.141T= MANE Select ENSP00000217260.4:p.Cys47=
ENST00000217260.8:c.141T= ENSP00000217260.4:p.Cys47=
ENST00000400634.2:c.141T= ENSP00000383475.2:p.Cys47=
NM_001029871.3:c.141T= NP_001025042.2:p.Cys47=
NM_001040007.2:c.141T= NP_001035096.1:p.Cys47=
XM_011529232.1:c.189T= XP_011527534.1:p.Cys63=
XM_011529233.1:c.189T= XP_011527535.1:p.Cys63=
XR_937068.1:n.261T=
XR_937069.1:n.256T=
XM_017027839.1:c.141T= XP_016883328.1:p.Cys47=
NM_001029871.4:c.141T= MANE Select NP_001025042.2:p.Cys47=
NM_001040007.3:c.141T= NP_001035096.1:p.Cys47=