Canonical Allele Identifier: CA509343656

Gene: RSPO4

Linked Data

• gnomAD v4: 20-968110-T-A
• MyVariant Identifiers: chr20:g.948753T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.968110T>A , CM000682.2:g.968110T>A	GRCh38
NC_000020.10:g.948753T>A , CM000682.1:g.948753T>A	GRCh37
NC_000020.9:g.896753T>A	NCBI36
NG_013043.1:g.39155A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217260.9:c.108A>T MANE Select	ENSP00000217260.4:p.Thr36=
ENST00000217260.8:c.108A>T	ENSP00000217260.4:p.Thr36=
ENST00000400634.2:c.108A>T	ENSP00000383475.2:p.Thr36=
NM_001029871.3:c.108A>T	NP_001025042.2:p.Thr36=
NM_001040007.2:c.108A>T	NP_001035096.1:p.Thr36=
XM_011529232.1:c.156A>T	XP_011527534.1:p.Thr52=
XM_011529233.1:c.156A>T	XP_011527535.1:p.Thr52=
XR_937068.1:n.228A>T
XR_937069.1:n.223A>T
XM_017027839.1:c.108A>T	XP_016883328.1:p.Thr36=
NM_001029871.4:c.108A>T MANE Select	NP_001025042.2:p.Thr36=
NM_001040007.3:c.108A>T	NP_001035096.1:p.Thr36=