Canonical Allele Identifier: CA407970321

Gene: RSPO4

Linked Data

• MyVariant Identifiers: chr20:g.948628A>T (hg19) ; chr20:g.967985A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967985A>T , CM000682.2:g.967985A>T	GRCh38
NC_000020.10:g.948628A>T , CM000682.1:g.948628A>T	GRCh37
NC_000020.9:g.896628A>T	NCBI36
NG_013043.1:g.39280T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.233T>A MANE Select	ENSP00000217260.4:p.Phe78Tyr
ENST00000217260.8:c.233T>A	ENSP00000217260.4:p.Phe78Tyr
ENST00000400634.2:c.233T>A	ENSP00000383475.2:p.Phe78Tyr
NM_001029871.3:c.233T>A	NP_001025042.2:p.Phe78Tyr
NM_001040007.2:c.233T>A	NP_001035096.1:p.Phe78Tyr
XM_011529232.1:c.281T>A	XP_011527534.1:p.Phe94Tyr
XM_011529233.1:c.281T>A	XP_011527535.1:p.Phe94Tyr
XR_937068.1:n.353T>A
XR_937069.1:n.348T>A
XM_017027839.1:c.233T>A	XP_016883328.1:p.Phe78Tyr
NM_001029871.4:c.233T>A MANE Select	NP_001025042.2:p.Phe78Tyr
NM_001040007.3:c.233T>A	NP_001035096.1:p.Phe78Tyr