Canonical Allele Identifier: CA2577315609
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968175del , CM000682.2:g.968175del GRCh38
NC_000020.10:g.948818del , CM000682.1:g.948818del GRCh37
NC_000020.9:g.896818del NCBI36
NG_013043.1:g.39092del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.80-35del MANE Select ENSP00000217260.4:n.80-35del
ENST00000217260.8:c.80-35del ENSP00000217260.4:n.80-35del
ENST00000400634.2:c.80-35del ENSP00000383475.2:n.80-35del
NM_001029871.3:c.80-35del NP_001025042.2:n.80-35del
NM_001040007.2:c.80-35del NP_001035096.1:n.80-35del
XM_011529232.1:c.128-35del XP_011527534.1:n.128-35del
XM_011529233.1:c.128-35del XP_011527535.1:n.128-35del
XR_937068.1:n.200-35del
XR_937069.1:n.195-35del
XM_017027839.1:c.80-35del XP_016883328.1:n.80-35del
NM_001029871.4:c.80-35del MANE Select NP_001025042.2:n.80-35del
NM_001040007.3:c.80-35del NP_001035096.1:n.80-35del