Canonical Allele Identifier: CA2345447849
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968006T= , CM000682.2:g.968006T= GRCh38
NC_000020.10:g.948649T= , CM000682.1:g.948649T= GRCh37
NC_000020.9:g.896649T= NCBI36
NG_013043.1:g.39259A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.212A= MANE Select ENSP00000217260.4:p.His71=
ENST00000217260.8:c.212A= ENSP00000217260.4:p.His71=
ENST00000400634.2:c.212A= ENSP00000383475.2:p.His71=
NM_001029871.3:c.212A= NP_001025042.2:p.His71=
NM_001040007.2:c.212A= NP_001035096.1:p.His71=
XM_011529232.1:c.260A= XP_011527534.1:p.His87=
XM_011529233.1:c.260A= XP_011527535.1:p.His87=
XR_937068.1:n.332A=
XR_937069.1:n.327A=
XM_017027839.1:c.212A= XP_016883328.1:p.His71=
NM_001029871.4:c.212A= MANE Select NP_001025042.2:p.His71=
NM_001040007.3:c.212A= NP_001035096.1:p.His71=