Canonical Allele Identifier: CA2651557873
Gene: RSPO4 HGNC NCBI

Linked Data

gnomAD v4: 20-968166-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.968166G>T , CM000682.2:g.968166G>T GRCh38
NC_000020.10:g.948809G>T , CM000682.1:g.948809G>T GRCh37
NC_000020.9:g.896809G>T NCBI36
NG_013043.1:g.39099C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000217260.9:c.80-28C>A MANE Select ENSP00000217260.4:n.80-28C>A
ENST00000217260.8:c.80-28C>A ENSP00000217260.4:n.80-28C>A
ENST00000400634.2:c.80-28C>A ENSP00000383475.2:n.80-28C>A
NM_001029871.3:c.80-28C>A NP_001025042.2:n.80-28C>A
NM_001040007.2:c.80-28C>A NP_001035096.1:n.80-28C>A
XM_011529232.1:c.128-28C>A XP_011527534.1:n.128-28C>A
XM_011529233.1:c.128-28C>A XP_011527535.1:n.128-28C>A
XR_937068.1:n.200-28C>A
XR_937069.1:n.195-28C>A
XM_017027839.1:c.80-28C>A XP_016883328.1:n.80-28C>A
NM_001029871.4:c.80-28C>A MANE Select NP_001025042.2:n.80-28C>A
NM_001040007.3:c.80-28C>A NP_001035096.1:n.80-28C>A