Canonical Allele Identifier: CA407970262

Gene: RSPO4

Linked Data

• dbSNP Id: rs1254735009
• MyVariant Identifiers: chr20:g.948616C>T (hg19) ; chr20:g.967973C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967973C>T , CM000682.2:g.967973C>T	GRCh38
NC_000020.10:g.948616C>T , CM000682.1:g.948616C>T	GRCh37
NC_000020.9:g.896616C>T	NCBI36
NG_013043.1:g.39292G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.245G>A MANE Select	ENSP00000217260.4:p.Gly82Asp
ENST00000217260.8:c.245G>A	ENSP00000217260.4:p.Gly82Asp
ENST00000400634.2:c.245G>A	ENSP00000383475.2:p.Gly82Asp
NM_001029871.3:c.245G>A	NP_001025042.2:p.Gly82Asp
NM_001040007.2:c.245G>A	NP_001035096.1:p.Gly82Asp
XM_011529232.1:c.293G>A	XP_011527534.1:p.Gly98Asp
XM_011529233.1:c.293G>A	XP_011527535.1:p.Gly98Asp
XR_937068.1:n.365G>A
XR_937069.1:n.360G>A
XM_017027839.1:c.245G>A	XP_016883328.1:p.Gly82Asp
NM_001029871.4:c.245G>A MANE Select	NP_001025042.2:p.Gly82Asp
NM_001040007.3:c.245G>A	NP_001035096.1:p.Gly82Asp