Canonical Allele Identifier: CA407970844
Gene: RSPO4 HGNC NCBI

Linked Data

dbSNP Id: rs1235248369
gnomAD v2: 20-948726-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968083G>C , CM000682.2:g.968083G>C GRCh38
NC_000020.10:g.948726G>C , CM000682.1:g.948726G>C GRCh37
NC_000020.9:g.896726G>C NCBI36
NG_013043.1:g.39182C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.135C>G MANE Select ENSP00000217260.4:p.Asn45Lys
ENST00000217260.8:c.135C>G ENSP00000217260.4:p.Asn45Lys
ENST00000400634.2:c.135C>G ENSP00000383475.2:p.Asn45Lys
NM_001029871.3:c.135C>G NP_001025042.2:p.Asn45Lys
NM_001040007.2:c.135C>G NP_001035096.1:p.Asn45Lys
XM_011529232.1:c.183C>G XP_011527534.1:p.Asn61Lys
XM_011529233.1:c.183C>G XP_011527535.1:p.Asn61Lys
XR_937068.1:n.255C>G
XR_937069.1:n.250C>G
XM_017027839.1:c.135C>G XP_016883328.1:p.Asn45Lys
NM_001029871.4:c.135C>G MANE Select NP_001025042.2:p.Asn45Lys
NM_001040007.3:c.135C>G NP_001035096.1:p.Asn45Lys