Canonical Allele Identifier: CA2695229187
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968053_968054delinsTT , CM000682.2:g.968053_968054delinsTT GRCh38
NC_000020.10:g.948696_948697delinsTT , CM000682.1:g.948696_948697delinsTT GRCh37
NC_000020.9:g.896696_896697delinsTT NCBI36
NG_013043.1:g.39211_39212delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.164_165delinsAA MANE Select ENSP00000217260.4:p.Phe55Ter
ENST00000217260.8:c.164_165delinsAA ENSP00000217260.4:p.Phe55Ter
ENST00000400634.2:c.164_165delinsAA ENSP00000383475.2:p.Phe55Ter
NM_001029871.3:c.164_165delinsAA NP_001025042.2:p.Phe55Ter
NM_001040007.2:c.164_165delinsAA NP_001035096.1:p.Phe55Ter
XM_011529232.1:c.212_213delinsAA XP_011527534.1:p.Phe71Ter
XM_011529233.1:c.212_213delinsAA XP_011527535.1:p.Phe71Ter
XR_937068.1:n.284_285delinsAA
XR_937069.1:n.279_280delinsAA
XM_017027839.1:c.164_165delinsAA XP_016883328.1:p.Phe55Ter
NM_001029871.4:c.164_165delinsAA MANE Select NP_001025042.2:p.Phe55Ter
NM_001040007.3:c.164_165delinsAA NP_001035096.1:p.Phe55Ter