Canonical Allele Identifier: CA407970956
Gene: RSPO4 HGNC NCBI

Linked Data

dbSNP Id: rs1271401983
gnomAD v3: 20-968102-A-T
gnomAD v4: 20-968102-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968102A>T , CM000682.2:g.968102A>T GRCh38
NC_000020.10:g.948745A>T , CM000682.1:g.948745A>T GRCh37
NC_000020.9:g.896745A>T NCBI36
NG_013043.1:g.39163T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.116T>A MANE Select ENSP00000217260.4:p.Ile39Asn
ENST00000217260.8:c.116T>A ENSP00000217260.4:p.Ile39Asn
ENST00000400634.2:c.116T>A ENSP00000383475.2:p.Ile39Asn
NM_001029871.3:c.116T>A NP_001025042.2:p.Ile39Asn
NM_001040007.2:c.116T>A NP_001035096.1:p.Ile39Asn
XM_011529232.1:c.164T>A XP_011527534.1:p.Ile55Asn
XM_011529233.1:c.164T>A XP_011527535.1:p.Ile55Asn
XR_937068.1:n.236T>A
XR_937069.1:n.231T>A
XM_017027839.1:c.116T>A XP_016883328.1:p.Ile39Asn
NM_001029871.4:c.116T>A MANE Select NP_001025042.2:p.Ile39Asn
NM_001040007.3:c.116T>A NP_001035096.1:p.Ile39Asn