Canonical Allele Identifier: CA968804410

Gene: SPRED1

Linked Data

• dbSNP Id: rs1895117045
• gnomAD v3: 15-38299782-A-ACT
• gnomAD v4: 15-38299782-A-ACT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299782_38299783insCT , CM000677.2:g.38299782_38299783insCT	GRCh38
NC_000015.9:g.38591983_38591984insCT , CM000677.1:g.38591983_38591984insCT	GRCh37
NC_000015.8:g.36379275_36379276insCT	NCBI36
NG_008980.1:g.51932_51933insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.207+235_207+236insCT MANE Select	ENSP00000299084.4:n.207+235_207+236insCT
ENST00000299084.8:c.207+235_207+236insCT	ENSP00000299084.4:n.207+235_207+236insCT
ENST00000561205.1:n.545+235_545+236insCT
ENST00000561317.1:c.144+235_144+236insCT	ENSP00000453680.1:n.144+235_144+236insCT
NM_152594.2:c.207+235_207+236insCT	NP_689807.1:n.207+235_207+236insCT
XM_005254202.2:c.243+235_243+236insCT	XP_005254259.1:n.243+235_243+236insCT
XM_005254203.3:c.-15-22459_-15-22458insCT	XP_005254260.1:n.-15-22459_-15-22458insCT
XM_011521288.1:c.144+235_144+236insCT	XP_011519590.1:n.144+235_144+236insCT
XM_011521289.1:c.144+235_144+236insCT	XP_011519591.1:n.144+235_144+236insCT
XM_011521290.1:c.144+235_144+236insCT	XP_011519592.1:n.144+235_144+236insCT
XM_005254202.3:c.243+235_243+236insCT	XP_005254259.1:n.243+235_243+236insCT
XM_011521289.3:c.144+235_144+236insCT	XP_011519591.1:n.144+235_144+236insCT
NM_152594.3:c.207+235_207+236insCT MANE Select	NP_689807.1:n.207+235_207+236insCT