Canonical Allele Identifier: CA407970956

Gene: RSPO4

Linked Data

• dbSNP Id: rs1271401983
• gnomAD v3: 20-968102-A-T
• gnomAD v4: 20-968102-A-T
• MyVariant Identifiers: chr20:g.948745A>T (hg19) ; chr20:g.968102A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.968102A>T , CM000682.2:g.968102A>T	GRCh38
NC_000020.10:g.948745A>T , CM000682.1:g.948745A>T	GRCh37
NC_000020.9:g.896745A>T	NCBI36
NG_013043.1:g.39163T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.116T>A MANE Select	ENSP00000217260.4:p.Ile39Asn
ENST00000217260.8:c.116T>A	ENSP00000217260.4:p.Ile39Asn
ENST00000400634.2:c.116T>A	ENSP00000383475.2:p.Ile39Asn
NM_001029871.3:c.116T>A	NP_001025042.2:p.Ile39Asn
NM_001040007.2:c.116T>A	NP_001035096.1:p.Ile39Asn
XM_011529232.1:c.164T>A	XP_011527534.1:p.Ile55Asn
XM_011529233.1:c.164T>A	XP_011527535.1:p.Ile55Asn
XR_937068.1:n.236T>A
XR_937069.1:n.231T>A
XM_017027839.1:c.116T>A	XP_016883328.1:p.Ile39Asn
NM_001029871.4:c.116T>A MANE Select	NP_001025042.2:p.Ile39Asn
NM_001040007.3:c.116T>A	NP_001035096.1:p.Ile39Asn