Canonical Allele Identifier: CA509343554

Gene: RSPO4

Linked Data

• MyVariant Identifiers: chr20:g.948639G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967996G>C , CM000682.2:g.967996G>C	GRCh38
NC_000020.10:g.948639G>C , CM000682.1:g.948639G>C	GRCh37
NC_000020.9:g.896639G>C	NCBI36
NG_013043.1:g.39269C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.222C>G MANE Select	ENSP00000217260.4:p.Pro74=
ENST00000217260.8:c.222C>G	ENSP00000217260.4:p.Pro74=
ENST00000400634.2:c.222C>G	ENSP00000383475.2:p.Pro74=
NM_001029871.3:c.222C>G	NP_001025042.2:p.Pro74=
NM_001040007.2:c.222C>G	NP_001035096.1:p.Pro74=
XM_011529232.1:c.270C>G	XP_011527534.1:p.Pro90=
XM_011529233.1:c.270C>G	XP_011527535.1:p.Pro90=
XR_937068.1:n.342C>G
XR_937069.1:n.337C>G
XM_017027839.1:c.222C>G	XP_016883328.1:p.Pro74=
NM_001029871.4:c.222C>G MANE Select	NP_001025042.2:p.Pro74=
NM_001040007.3:c.222C>G	NP_001035096.1:p.Pro74=