Canonical Allele Identifier: CA407970404
Gene: RSPO4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968000C>A , CM000682.2:g.968000C>A GRCh38
NC_000020.10:g.948643C>A , CM000682.1:g.948643C>A GRCh37
NC_000020.9:g.896643C>A NCBI36
NG_013043.1:g.39265G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.218G>T MANE Select ENSP00000217260.4:p.Cys73Phe
ENST00000217260.8:c.218G>T ENSP00000217260.4:p.Cys73Phe
ENST00000400634.2:c.218G>T ENSP00000383475.2:p.Cys73Phe
NM_001029871.3:c.218G>T NP_001025042.2:p.Cys73Phe
NM_001040007.2:c.218G>T NP_001035096.1:p.Cys73Phe
XM_011529232.1:c.266G>T XP_011527534.1:p.Cys89Phe
XM_011529233.1:c.266G>T XP_011527535.1:p.Cys89Phe
XR_937068.1:n.338G>T
XR_937069.1:n.333G>T
XM_017027839.1:c.218G>T XP_016883328.1:p.Cys73Phe
NM_001029871.4:c.218G>T MANE Select NP_001025042.2:p.Cys73Phe
NM_001040007.3:c.218G>T NP_001035096.1:p.Cys73Phe