Canonical Allele Identifier: CA2345447751
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968347A= , CM000682.2:g.968347A= GRCh38
NC_000020.10:g.948990A= , CM000682.1:g.948990A= GRCh37
NC_000020.9:g.896990A= NCBI36
NG_013043.1:g.38918T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.80-209T= MANE Select ENSP00000217260.4:n.80-209T=
ENST00000217260.8:c.80-209T= ENSP00000217260.4:n.80-209T=
ENST00000400634.2:c.80-209T= ENSP00000383475.2:n.80-209T=
NM_001029871.3:c.80-209T= NP_001025042.2:n.80-209T=
NM_001040007.2:c.80-209T= NP_001035096.1:n.80-209T=
XM_011529232.1:c.128-209T= XP_011527534.1:n.128-209T=
XM_011529233.1:c.128-209T= XP_011527535.1:n.128-209T=
XR_937068.1:n.200-209T=
XR_937069.1:n.195-209T=
XM_017027839.1:c.80-209T= XP_016883328.1:n.80-209T=
NM_001029871.4:c.80-209T= MANE Select NP_001025042.2:n.80-209T=
NM_001040007.3:c.80-209T= NP_001035096.1:n.80-209T=