Canonical Allele Identifier: CA407970792

Gene: RSPO4

Linked Data

• MyVariant Identifiers: chr20:g.948716T>A (hg19) ; chr20:g.968073T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.145A>T MANE Select	ENSP00000217260.4:p.Thr49Ser
ENST00000217260.8:c.145A>T	ENSP00000217260.4:p.Thr49Ser
ENST00000400634.2:c.145A>T	ENSP00000383475.2:p.Thr49Ser
NM_001029871.3:c.145A>T	NP_001025042.2:p.Thr49Ser
NM_001040007.2:c.145A>T	NP_001035096.1:p.Thr49Ser
XM_011529232.1:c.193A>T	XP_011527534.1:p.Thr65Ser
XM_011529233.1:c.193A>T	XP_011527535.1:p.Thr65Ser
XR_937068.1:n.265A>T
XR_937069.1:n.260A>T
XM_017027839.1:c.145A>T	XP_016883328.1:p.Thr49Ser
NM_001029871.4:c.145A>T MANE Select	NP_001025042.2:p.Thr49Ser
NM_001040007.3:c.145A>T	NP_001035096.1:p.Thr49Ser