Canonical Allele Identifier: CA407970935

Gene: RSPO4

Linked Data

• MyVariant Identifiers: chr20:g.948742A>C (hg19) ; chr20:g.968099A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.968099A>C , CM000682.2:g.968099A>C	GRCh38
NC_000020.10:g.948742A>C , CM000682.1:g.948742A>C	GRCh37
NC_000020.9:g.896742A>C	NCBI36
NG_013043.1:g.39166T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.119T>G MANE Select	ENSP00000217260.4:p.Ile40Ser
ENST00000217260.8:c.119T>G	ENSP00000217260.4:p.Ile40Ser
ENST00000400634.2:c.119T>G	ENSP00000383475.2:p.Ile40Ser
NM_001029871.3:c.119T>G	NP_001025042.2:p.Ile40Ser
NM_001040007.2:c.119T>G	NP_001035096.1:p.Ile40Ser
XM_011529232.1:c.167T>G	XP_011527534.1:p.Ile56Ser
XM_011529233.1:c.167T>G	XP_011527535.1:p.Ile56Ser
XR_937068.1:n.239T>G
XR_937069.1:n.234T>G
XM_017027839.1:c.119T>G	XP_016883328.1:p.Ile40Ser
NM_001029871.4:c.119T>G MANE Select	NP_001025042.2:p.Ile40Ser
NM_001040007.3:c.119T>G	NP_001035096.1:p.Ile40Ser