Canonical Allele Identifier: CA2815014481
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968260_968261insCAACCA , CM000682.2:g.968260_968261insCAACCA GRCh38
NC_000020.10:g.948903_948904insCAACCA , CM000682.1:g.948903_948904insCAACCA GRCh37
NC_000020.9:g.896903_896904insCAACCA NCBI36
NG_013043.1:g.39005_39006insGGTTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.80-122_80-121insGGTTGT MANE Select ENSP00000217260.4:n.80-122_80-121insGGTTGT
ENST00000217260.8:c.80-122_80-121insGGTTGT ENSP00000217260.4:n.80-122_80-121insGGTTGT
ENST00000400634.2:c.80-122_80-121insGGTTGT ENSP00000383475.2:n.80-122_80-121insGGTTGT
NM_001029871.3:c.80-122_80-121insGGTTGT NP_001025042.2:n.80-122_80-121insGGTTGT
NM_001040007.2:c.80-122_80-121insGGTTGT NP_001035096.1:n.80-122_80-121insGGTTGT
XM_011529232.1:c.128-122_128-121insGGTTGT XP_011527534.1:n.128-122_128-121insGGTTGT
XM_011529233.1:c.128-122_128-121insGGTTGT XP_011527535.1:n.128-122_128-121insGGTTGT
XR_937068.1:n.200-122_200-121insGGTTGT
XR_937069.1:n.195-122_195-121insGGTTGT
XM_017027839.1:c.80-122_80-121insGGTTGT XP_016883328.1:n.80-122_80-121insGGTTGT
NM_001029871.4:c.80-122_80-121insGGTTGT MANE Select NP_001025042.2:n.80-122_80-121insGGTTGT
NM_001040007.3:c.80-122_80-121insGGTTGT NP_001035096.1:n.80-122_80-121insGGTTGT