Canonical Allele Identifier: CA2651557991

Gene: RSPO4

Linked Data

• gnomAD v4: 20-968240-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.968240C>T , CM000682.2:g.968240C>T	GRCh38
NC_000020.10:g.948883C>T , CM000682.1:g.948883C>T	GRCh37
NC_000020.9:g.896883C>T	NCBI36
NG_013043.1:g.39025G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.80-102G>A MANE Select	ENSP00000217260.4:n.80-102G>A
ENST00000217260.8:c.80-102G>A	ENSP00000217260.4:n.80-102G>A
ENST00000400634.2:c.80-102G>A	ENSP00000383475.2:n.80-102G>A
NM_001029871.3:c.80-102G>A	NP_001025042.2:n.80-102G>A
NM_001040007.2:c.80-102G>A	NP_001035096.1:n.80-102G>A
XM_011529232.1:c.128-102G>A	XP_011527534.1:n.128-102G>A
XM_011529233.1:c.128-102G>A	XP_011527535.1:n.128-102G>A
XR_937068.1:n.200-102G>A
XR_937069.1:n.195-102G>A
XM_017027839.1:c.80-102G>A	XP_016883328.1:n.80-102G>A
NM_001029871.4:c.80-102G>A MANE Select	NP_001025042.2:n.80-102G>A
NM_001040007.3:c.80-102G>A	NP_001035096.1:n.80-102G>A