Canonical Allele Identifier: CA968804368

Gene: SPRED1

Linked Data

• gnomAD v3: 15-38299716-G-GTTTTTTTTT
• gnomAD v4: 15-38299716-G-GTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299716_38299717insTTTTTTTTT , CM000677.2:g.38299716_38299717insTTTTTTTTT	GRCh38
NC_000015.9:g.38591917_38591918insTTTTTTTTT , CM000677.1:g.38591917_38591918insTTTTTTTTT	GRCh37
NC_000015.8:g.36379209_36379210insTTTTTTTTT	NCBI36
NG_008980.1:g.51866_51867insTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.207+169_207+170insTTTTTTTTT MANE Select	ENSP00000299084.4:n.207+169_207+170insTTTTTTTTT
ENST00000299084.8:c.207+169_207+170insTTTTTTTTT	ENSP00000299084.4:n.207+169_207+170insTTTTTTTTT
ENST00000561205.1:n.545+169_545+170insTTTTTTTTT
ENST00000561317.1:c.144+169_144+170insTTTTTTTTT	ENSP00000453680.1:n.144+169_144+170insTTTTTTTTT
NM_152594.2:c.207+169_207+170insTTTTTTTTT	NP_689807.1:n.207+169_207+170insTTTTTTTTT
XM_005254202.2:c.243+169_243+170insTTTTTTTTT	XP_005254259.1:n.243+169_243+170insTTTTTTTTT
XM_005254203.3:c.-15-22525_-15-22524insTTTTTTTTT	XP_005254260.1:n.-15-22525_-15-22524insTTTTTTTTT
XM_011521288.1:c.144+169_144+170insTTTTTTTTT	XP_011519590.1:n.144+169_144+170insTTTTTTTTT
XM_011521289.1:c.144+169_144+170insTTTTTTTTT	XP_011519591.1:n.144+169_144+170insTTTTTTTTT
XM_011521290.1:c.144+169_144+170insTTTTTTTTT	XP_011519592.1:n.144+169_144+170insTTTTTTTTT
XM_005254202.3:c.243+169_243+170insTTTTTTTTT	XP_005254259.1:n.243+169_243+170insTTTTTTTTT
XM_011521289.3:c.144+169_144+170insTTTTTTTTT	XP_011519591.1:n.144+169_144+170insTTTTTTTTT
NM_152594.3:c.207+169_207+170insTTTTTTTTT MANE Select	NP_689807.1:n.207+169_207+170insTTTTTTTTT