Canonical Allele Identifier: CA2832575273
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.967998dup , CM000682.2:g.967998dup GRCh38
NC_000020.10:g.948641dup , CM000682.1:g.948641dup GRCh37
NC_000020.9:g.896641dup NCBI36
NG_013043.1:g.39271dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.224dup MANE Select ENSP00000217260.4:p.Gly76TrpfsTer21
ENST00000217260.8:c.224dup ENSP00000217260.4:p.Gly76TrpfsTer21
ENST00000400634.2:c.224dup ENSP00000383475.2:p.Gly76TrpfsTer21
NM_001029871.3:c.224dup NP_001025042.2:p.Gly76TrpfsTer21
NM_001040007.2:c.224dup NP_001035096.1:p.Gly76TrpfsTer21
XM_011529232.1:c.272dup XP_011527534.1:p.Gly92TrpfsTer21
XM_011529233.1:c.272dup XP_011527535.1:p.Gly92TrpfsTer21
XR_937068.1:n.344dup
XR_937069.1:n.339dup
XM_017027839.1:c.224dup XP_016883328.1:p.Gly76TrpfsTer21
NM_001029871.4:c.224dup MANE Select NP_001025042.2:p.Gly76TrpfsTer21
NM_001040007.3:c.224dup NP_001035096.1:p.Gly76TrpfsTer21