Canonical Allele Identifier: CA509343633

Gene: RSPO4

Linked Data

• MyVariant Identifiers: chr20:g.948714G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.968071G>A , CM000682.2:g.968071G>A	GRCh38
NC_000020.10:g.948714G>A , CM000682.1:g.948714G>A	GRCh37
NC_000020.9:g.896714G>A	NCBI36
NG_013043.1:g.39194C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.147C>T MANE Select	ENSP00000217260.4:p.Thr49=
ENST00000217260.8:c.147C>T	ENSP00000217260.4:p.Thr49=
ENST00000400634.2:c.147C>T	ENSP00000383475.2:p.Thr49=
NM_001029871.3:c.147C>T	NP_001025042.2:p.Thr49=
NM_001040007.2:c.147C>T	NP_001035096.1:p.Thr49=
XM_011529232.1:c.195C>T	XP_011527534.1:p.Thr65=
XM_011529233.1:c.195C>T	XP_011527535.1:p.Thr65=
XR_937068.1:n.267C>T
XR_937069.1:n.262C>T
XM_017027839.1:c.147C>T	XP_016883328.1:p.Thr49=
NM_001029871.4:c.147C>T MANE Select	NP_001025042.2:p.Thr49=
NM_001040007.3:c.147C>T	NP_001035096.1:p.Thr49=