Canonical Allele Identifier: CA2815014480
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968257_968258insCACCCAACAC , CM000682.2:g.968257_968258insCACCCAACAC GRCh38
NC_000020.10:g.948900_948901insCACCCAACAC , CM000682.1:g.948900_948901insCACCCAACAC GRCh37
NC_000020.9:g.896900_896901insCACCCAACAC NCBI36
NG_013043.1:g.39007_39008insGTGTTGGGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.80-120_80-119insGTGTTGGGTG MANE Select ENSP00000217260.4:n.80-120_80-119insGTGTTGGGTG
ENST00000217260.8:c.80-120_80-119insGTGTTGGGTG ENSP00000217260.4:n.80-120_80-119insGTGTTGGGTG
ENST00000400634.2:c.80-120_80-119insGTGTTGGGTG ENSP00000383475.2:n.80-120_80-119insGTGTTGGGTG
NM_001029871.3:c.80-120_80-119insGTGTTGGGTG NP_001025042.2:n.80-120_80-119insGTGTTGGGTG
NM_001040007.2:c.80-120_80-119insGTGTTGGGTG NP_001035096.1:n.80-120_80-119insGTGTTGGGTG
XM_011529232.1:c.128-120_128-119insGTGTTGGGTG XP_011527534.1:n.128-120_128-119insGTGTTGGGTG
XM_011529233.1:c.128-120_128-119insGTGTTGGGTG XP_011527535.1:n.128-120_128-119insGTGTTGGGTG
XR_937068.1:n.200-120_200-119insGTGTTGGGTG
XR_937069.1:n.195-120_195-119insGTGTTGGGTG
XM_017027839.1:c.80-120_80-119insGTGTTGGGTG XP_016883328.1:n.80-120_80-119insGTGTTGGGTG
NM_001029871.4:c.80-120_80-119insGTGTTGGGTG MANE Select NP_001025042.2:n.80-120_80-119insGTGTTGGGTG
NM_001040007.3:c.80-120_80-119insGTGTTGGGTG NP_001035096.1:n.80-120_80-119insGTGTTGGGTG