Canonical Allele Identifier: CA2345447816
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.967996G= , CM000682.2:g.967996G= GRCh38
NC_000020.10:g.948639G= , CM000682.1:g.948639G= GRCh37
NC_000020.9:g.896639G= NCBI36
NG_013043.1:g.39269C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.222C= MANE Select ENSP00000217260.4:p.Pro74=
ENST00000217260.8:c.222C= ENSP00000217260.4:p.Pro74=
ENST00000400634.2:c.222C= ENSP00000383475.2:p.Pro74=
NM_001029871.3:c.222C= NP_001025042.2:p.Pro74=
NM_001040007.2:c.222C= NP_001035096.1:p.Pro74=
XM_011529232.1:c.270C= XP_011527534.1:p.Pro90=
XM_011529233.1:c.270C= XP_011527535.1:p.Pro90=
XR_937068.1:n.342C=
XR_937069.1:n.337C=
XM_017027839.1:c.222C= XP_016883328.1:p.Pro74=
NM_001029871.4:c.222C= MANE Select NP_001025042.2:p.Pro74=
NM_001040007.3:c.222C= NP_001035096.1:p.Pro74=