Canonical Allele Identifier: CA2345447519
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.967790C= , CM000682.2:g.967790C= GRCh38
NC_000020.10:g.948433C= , CM000682.1:g.948433C= GRCh37
NC_000020.9:g.896433C= NCBI36
NG_013043.1:g.39475G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.268+160G= MANE Select ENSP00000217260.4:n.268+160G=
ENST00000217260.8:c.268+160G= ENSP00000217260.4:n.268+160G=
ENST00000400634.2:c.268+160G= ENSP00000383475.2:n.268+160G=
NM_001029871.3:c.268+160G= NP_001025042.2:n.268+160G=
NM_001040007.2:c.268+160G= NP_001035096.1:n.268+160G=
XM_011529232.1:c.316+160G= XP_011527534.1:n.316+160G=
XM_011529233.1:c.316+160G= XP_011527535.1:n.316+160G=
XR_937068.1:n.388+160G=
XR_937069.1:n.383+160G=
XM_017027839.1:c.268+160G= XP_016883328.1:n.268+160G=
NM_001029871.4:c.268+160G= MANE Select NP_001025042.2:n.268+160G=
NM_001040007.3:c.268+160G= NP_001035096.1:n.268+160G=