Canonical Allele Identifier: CA2345447489

Gene: RSPO4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.968073T= , CM000682.2:g.968073T=	GRCh38
NC_000020.10:g.948716T= , CM000682.1:g.948716T=	GRCh37
NC_000020.9:g.896716T=	NCBI36
NG_013043.1:g.39192A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.145A= MANE Select	ENSP00000217260.4:p.Thr49=
ENST00000217260.8:c.145A=	ENSP00000217260.4:p.Thr49=
ENST00000400634.2:c.145A=	ENSP00000383475.2:p.Thr49=
NM_001029871.3:c.145A=	NP_001025042.2:p.Thr49=
NM_001040007.2:c.145A=	NP_001035096.1:p.Thr49=
XM_011529232.1:c.193A=	XP_011527534.1:p.Thr65=
XM_011529233.1:c.193A=	XP_011527535.1:p.Thr65=
XR_937068.1:n.265A=
XR_937069.1:n.260A=
XM_017027839.1:c.145A=	XP_016883328.1:p.Thr49=
NM_001029871.4:c.145A= MANE Select	NP_001025042.2:p.Thr49=
NM_001040007.3:c.145A=	NP_001035096.1:p.Thr49=