Canonical Allele Identifier: CA2651557641
Gene: RSPO4 HGNC NCBI

Linked Data

gnomAD v4: 20-967834-TG-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.967837del , CM000682.2:g.967837del GRCh38
NC_000020.10:g.948480del , CM000682.1:g.948480del GRCh37
NC_000020.9:g.896480del NCBI36
NG_013043.1:g.39430del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.268+115del MANE Select ENSP00000217260.4:n.268+115del
ENST00000217260.8:c.268+115del ENSP00000217260.4:n.268+115del
ENST00000400634.2:c.268+115del ENSP00000383475.2:n.268+115del
NM_001029871.3:c.268+115del NP_001025042.2:n.268+115del
NM_001040007.2:c.268+115del NP_001035096.1:n.268+115del
XM_011529232.1:c.316+115del XP_011527534.1:n.316+115del
XM_011529233.1:c.316+115del XP_011527535.1:n.316+115del
XR_937068.1:n.388+115del
XR_937069.1:n.383+115del
XM_017027839.1:c.268+115del XP_016883328.1:n.268+115del
NM_001029871.4:c.268+115del MANE Select NP_001025042.2:n.268+115del
NM_001040007.3:c.268+115del NP_001035096.1:n.268+115del