Canonical Allele Identifier: CA746832440

Gene: RSPO4

Linked Data

• dbSNP Id: rs1462368152
• gnomAD v4: 20-967852-T-TA
• MyVariant Identifiers: chr20:g.948495_948496insA (hg19) ; chr20:g.967852_967853insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967853dup , CM000682.2:g.967853dup	GRCh38
NC_000020.10:g.948496dup , CM000682.1:g.948496dup	GRCh37
NC_000020.9:g.896496dup	NCBI36
NG_013043.1:g.39412dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.268+97dup MANE Select	ENSP00000217260.4:n.268+97dup
ENST00000217260.8:c.268+97dup	ENSP00000217260.4:n.268+97dup
ENST00000400634.2:c.268+97dup	ENSP00000383475.2:n.268+97dup
NM_001029871.3:c.268+97dup	NP_001025042.2:n.268+97dup
NM_001040007.2:c.268+97dup	NP_001035096.1:n.268+97dup
XM_011529232.1:c.316+97dup	XP_011527534.1:n.316+97dup
XM_011529233.1:c.316+97dup	XP_011527535.1:n.316+97dup
XR_937068.1:n.388+97dup
XR_937069.1:n.383+97dup
XM_017027839.1:c.268+97dup	XP_016883328.1:n.268+97dup
NM_001029871.4:c.268+97dup MANE Select	NP_001025042.2:n.268+97dup
NM_001040007.3:c.268+97dup	NP_001035096.1:n.268+97dup