Canonical Allele Identifier: CA2345447253
Community Standard Title: NM_001029871.4(RSPO4):c.319T= (p.Cys107=)
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.967264A= , CM000682.2:g.967264A= GRCh38
NC_000020.10:g.947907A= , CM000682.1:g.947907A= GRCh37
NC_000020.9:g.895907A= NCBI36
NG_013043.1:g.40001T=

Transcript Alleles

HGVS Amino-acid Change
NM_001029871.4:c.319T= MANE Select NP_001025042.2:p.Cys107=
ENST00000217260.9:c.319T= MANE Select ENSP00000217260.4:p.Cys107=
NM_001029871.3:c.319T= NP_001025042.2:p.Cys107=
NM_001040007.2:c.319T= NP_001035096.1:p.Cys107=
NM_001040007.3:c.319T= NP_001035096.1:p.Cys107=
ENST00000217260.8:c.319T= ENSP00000217260.4:p.Cys107=
ENST00000400634.2:c.319T= ENSP00000383475.2:p.Cys107=
XM_011529232.1:c.367T= XP_011527534.1:p.Cys123=
XM_011529233.1:c.367T= XP_011527535.1:p.Cys123=
XM_017027839.1:c.319T= XP_016883328.1:p.Cys107=
XR_937068.1:n.439T=
XR_937069.1:n.434T=