Canonical Allele Identifier: CA2345447587

Gene: RSPO4

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.967871_967872delinsCT , CM000682.2:g.967871_967872delinsCT	GRCh38
NC_000020.10:g.948514_948515delinsCT , CM000682.1:g.948514_948515delinsCT	GRCh37
NC_000020.9:g.896514_896515delinsCT	NCBI36
NG_013043.1:g.39393_39394delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.268+78_268+79delinsAG MANE Select	ENSP00000217260.4:n.268+78_268+79delinsAG
ENST00000217260.8:c.268+78_268+79delinsAG	ENSP00000217260.4:n.268+78_268+79delinsAG
ENST00000400634.2:c.268+78_268+79delinsAG	ENSP00000383475.2:n.268+78_268+79delinsAG
NM_001029871.3:c.268+78_268+79delinsAG	NP_001025042.2:n.268+78_268+79delinsAG
NM_001040007.2:c.268+78_268+79delinsAG	NP_001035096.1:n.268+78_268+79delinsAG
XM_011529232.1:c.316+78_316+79delinsAG	XP_011527534.1:n.316+78_316+79delinsAG
XM_011529233.1:c.316+78_316+79delinsAG	XP_011527535.1:n.316+78_316+79delinsAG
XR_937068.1:n.388+78_388+79delinsAG
XR_937069.1:n.383+78_383+79delinsAG
XM_017027839.1:c.268+78_268+79delinsAG	XP_016883328.1:n.268+78_268+79delinsAG
NM_001029871.4:c.268+78_268+79delinsAG MANE Select	NP_001025042.2:n.268+78_268+79delinsAG
NM_001040007.3:c.268+78_268+79delinsAG	NP_001035096.1:n.268+78_268+79delinsAG