Canonical Allele Identifier: CA407971098

Gene: RSPO4

Linked Data

• MyVariant Identifiers: chr20:g.948773C>T (hg19) ; chr20:g.968130C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.968130C>T , CM000682.2:g.968130C>T	GRCh38
NC_000020.10:g.948773C>T , CM000682.1:g.948773C>T	GRCh37
NC_000020.9:g.896773C>T	NCBI36
NG_013043.1:g.39135G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.88G>A MANE Select	ENSP00000217260.4:p.Gly30Ser
ENST00000217260.8:c.88G>A	ENSP00000217260.4:p.Gly30Ser
ENST00000400634.2:c.88G>A	ENSP00000383475.2:p.Gly30Ser
NM_001029871.3:c.88G>A	NP_001025042.2:p.Gly30Ser
NM_001040007.2:c.88G>A	NP_001035096.1:p.Gly30Ser
XM_011529232.1:c.136G>A	XP_011527534.1:p.Gly46Ser
XM_011529233.1:c.136G>A	XP_011527535.1:p.Gly46Ser
XR_937068.1:n.208G>A
XR_937069.1:n.203G>A
XM_017027839.1:c.88G>A	XP_016883328.1:p.Gly30Ser
NM_001029871.4:c.88G>A MANE Select	NP_001025042.2:p.Gly30Ser
NM_001040007.3:c.88G>A	NP_001035096.1:p.Gly30Ser