Canonical Allele Identifier: CA2651557987
Gene: RSPO4 HGNC NCBI

Linked Data

gnomAD v4: 20-968238-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968238G>C , CM000682.2:g.968238G>C GRCh38
NC_000020.10:g.948881G>C , CM000682.1:g.948881G>C GRCh37
NC_000020.9:g.896881G>C NCBI36
NG_013043.1:g.39027C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.80-100C>G MANE Select ENSP00000217260.4:n.80-100C>G
ENST00000217260.8:c.80-100C>G ENSP00000217260.4:n.80-100C>G
ENST00000400634.2:c.80-100C>G ENSP00000383475.2:n.80-100C>G
NM_001029871.3:c.80-100C>G NP_001025042.2:n.80-100C>G
NM_001040007.2:c.80-100C>G NP_001035096.1:n.80-100C>G
XM_011529232.1:c.128-100C>G XP_011527534.1:n.128-100C>G
XM_011529233.1:c.128-100C>G XP_011527535.1:n.128-100C>G
XR_937068.1:n.200-100C>G
XR_937069.1:n.195-100C>G
XM_017027839.1:c.80-100C>G XP_016883328.1:n.80-100C>G
NM_001029871.4:c.80-100C>G MANE Select NP_001025042.2:n.80-100C>G
NM_001040007.3:c.80-100C>G NP_001035096.1:n.80-100C>G