Canonical Allele Identifier: CA2345447911
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968024T= , CM000682.2:g.968024T= GRCh38
NC_000020.10:g.948667T= , CM000682.1:g.948667T= GRCh37
NC_000020.9:g.896667T= NCBI36
NG_013043.1:g.39241A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.194A= MANE Select ENSP00000217260.4:p.Gln65=
ENST00000217260.8:c.194A= ENSP00000217260.4:p.Gln65=
ENST00000400634.2:c.194A= ENSP00000383475.2:p.Gln65=
NM_001029871.3:c.194A= NP_001025042.2:p.Gln65=
NM_001040007.2:c.194A= NP_001035096.1:p.Gln65=
XM_011529232.1:c.242A= XP_011527534.1:p.Gln81=
XM_011529233.1:c.242A= XP_011527535.1:p.Gln81=
XR_937068.1:n.314A=
XR_937069.1:n.309A=
XM_017027839.1:c.194A= XP_016883328.1:p.Gln65=
NM_001029871.4:c.194A= MANE Select NP_001025042.2:p.Gln65=
NM_001040007.3:c.194A= NP_001035096.1:p.Gln65=