Canonical Allele Identifier: CA2345447534
Gene: RSPO4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.967800A= , CM000682.2:g.967800A= GRCh38
NC_000020.10:g.948443A= , CM000682.1:g.948443A= GRCh37
NC_000020.9:g.896443A= NCBI36
NG_013043.1:g.39465T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.268+150T= MANE Select ENSP00000217260.4:n.268+150T=
ENST00000217260.8:c.268+150T= ENSP00000217260.4:n.268+150T=
ENST00000400634.2:c.268+150T= ENSP00000383475.2:n.268+150T=
NM_001029871.3:c.268+150T= NP_001025042.2:n.268+150T=
NM_001040007.2:c.268+150T= NP_001035096.1:n.268+150T=
XM_011529232.1:c.316+150T= XP_011527534.1:n.316+150T=
XM_011529233.1:c.316+150T= XP_011527535.1:n.316+150T=
XR_937068.1:n.388+150T=
XR_937069.1:n.383+150T=
XM_017027839.1:c.268+150T= XP_016883328.1:n.268+150T=
NM_001029871.4:c.268+150T= MANE Select NP_001025042.2:n.268+150T=
NM_001040007.3:c.268+150T= NP_001035096.1:n.268+150T=