Canonical Allele Identifier: CA968807458

Gene: SPRED1

Linked Data

• gnomAD v3: 15-38253258-C-CTTTTAAACT
• gnomAD v4: 15-38253258-C-CTTTTAAACT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253259_38253260insTTTAAACTT , CM000677.2:g.38253259_38253260insTTTAAACTT	GRCh38
NC_000015.9:g.38545460_38545461insTTTAAACTT , CM000677.1:g.38545460_38545461insTTTAAACTT	GRCh37
NC_000015.8:g.36332752_36332753insTTTAAACTT	NCBI36
NG_008980.1:g.5409_5410insTTTAAACTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.32+42_32+43insTTTAAACTT MANE Select	ENSP00000299084.4:n.32+42_32+43insTTTAAACTT
ENST00000299084.8:c.32+42_32+43insTTTAAACTT	ENSP00000299084.4:n.32+42_32+43insTTTAAACTT
ENST00000561205.1:n.370+42_370+43insTTTAAACTT
ENST00000561317.1:c.-96+42_-96+43insTTTAAACTT	ENSP00000453680.1:n.-96+42_-96+43insTTTAAACTT
NM_152594.2:c.32+42_32+43insTTTAAACTT	NP_689807.1:n.32+42_32+43insTTTAAACTT
XM_005254202.2:c.32+42_32+43insTTTAAACTT	XP_005254259.1:n.32+42_32+43insTTTAAACTT
XM_005254203.3:c.-16+42_-16+43insTTTAAACTT	XP_005254260.1:n.-16+42_-16+43insTTTAAACTT
XM_005254202.3:c.32+42_32+43insTTTAAACTT	XP_005254259.1:n.32+42_32+43insTTTAAACTT
XR_001751484.1:n.87+308_87+309insAGTTTAAAA
NM_152594.3:c.32+42_32+43insTTTAAACTT MANE Select	NP_689807.1:n.32+42_32+43insTTTAAACTT