Canonical Allele Identifier: CA407970371
Gene: RSPO4 HGNC NCBI

Linked Data

gnomAD v4: 20-967994-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.967994G>A , CM000682.2:g.967994G>A GRCh38
NC_000020.10:g.948637G>A , CM000682.1:g.948637G>A GRCh37
NC_000020.9:g.896637G>A NCBI36
NG_013043.1:g.39271C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.224C>T MANE Select ENSP00000217260.4:p.Pro75Leu
ENST00000217260.8:c.224C>T ENSP00000217260.4:p.Pro75Leu
ENST00000400634.2:c.224C>T ENSP00000383475.2:p.Pro75Leu
NM_001029871.3:c.224C>T NP_001025042.2:p.Pro75Leu
NM_001040007.2:c.224C>T NP_001035096.1:p.Pro75Leu
XM_011529232.1:c.272C>T XP_011527534.1:p.Pro91Leu
XM_011529233.1:c.272C>T XP_011527535.1:p.Pro91Leu
XR_937068.1:n.344C>T
XR_937069.1:n.339C>T
XM_017027839.1:c.224C>T XP_016883328.1:p.Pro75Leu
NM_001029871.4:c.224C>T MANE Select NP_001025042.2:p.Pro75Leu
NM_001040007.3:c.224C>T NP_001035096.1:p.Pro75Leu