Canonical Allele Identifier: CA407970592
Gene: RSPO4 HGNC NCBI

Linked Data

dbSNP Id: rs1568909897

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968036T>C , CM000682.2:g.968036T>C GRCh38
NC_000020.10:g.948679T>C , CM000682.1:g.948679T>C GRCh37
NC_000020.9:g.896679T>C NCBI36
NG_013043.1:g.39229A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.182A>G MANE Select ENSP00000217260.4:p.Glu61Gly
ENST00000217260.8:c.182A>G ENSP00000217260.4:p.Glu61Gly
ENST00000400634.2:c.182A>G ENSP00000383475.2:p.Glu61Gly
NM_001029871.3:c.182A>G NP_001025042.2:p.Glu61Gly
NM_001040007.2:c.182A>G NP_001035096.1:p.Glu61Gly
XM_011529232.1:c.230A>G XP_011527534.1:p.Glu77Gly
XM_011529233.1:c.230A>G XP_011527535.1:p.Glu77Gly
XR_937068.1:n.302A>G
XR_937069.1:n.297A>G
XM_017027839.1:c.182A>G XP_016883328.1:p.Glu61Gly
NM_001029871.4:c.182A>G MANE Select NP_001025042.2:p.Glu61Gly
NM_001040007.3:c.182A>G NP_001035096.1:p.Glu61Gly