Canonical Allele Identifier: CA645611897
Gene: RSPO4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968070_968073del , CM000682.2:g.968070_968073del GRCh38
NC_000020.10:g.948713_948716del , CM000682.1:g.948713_948716del GRCh37
NC_000020.9:g.896713_896716del NCBI36
NG_013043.1:g.39192_39195del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.145_148del MANE Select ENSP00000217260.4:p.Thr49AlafsTer?
ENST00000217260.8:c.145_148del ENSP00000217260.4:p.Thr49AlafsTer?
ENST00000400634.2:c.145_148del ENSP00000383475.2:p.Thr49AlafsTer?
NM_001029871.3:c.145_148del NP_001025042.2:p.Thr49AlafsTer?
NM_001040007.2:c.145_148del NP_001035096.1:p.Thr49AlafsTer?
XM_011529232.1:c.193_196del XP_011527534.1:p.Thr65AlafsTer?
XM_011529233.1:c.193_196del XP_011527535.1:p.Thr65AlafsTer?
XR_937068.1:n.265_268del
XR_937069.1:n.260_263del
XM_017027839.1:c.145_148del XP_016883328.1:p.Thr49AlafsTer?
NM_001029871.4:c.145_148del MANE Select NP_001025042.2:p.Thr49AlafsTer?
NM_001040007.3:c.145_148del NP_001035096.1:p.Thr49AlafsTer?