Canonical Allele Identifier: CA968804092

Gene: SPRED1

Linked Data

• dbSNP Id: rs1895101612
• gnomAD v3: 15-38299224-GCTA-G
• gnomAD v4: 15-38299224-GCTA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299227_38299229del , CM000677.2:g.38299227_38299229del	GRCh38
NC_000015.9:g.38591428_38591430del , CM000677.1:g.38591428_38591430del	GRCh37
NC_000015.8:g.36378720_36378722del	NCBI36
NG_008980.1:g.51377_51379del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.33-146_33-144del MANE Select	ENSP00000299084.4:n.33-146_33-144del
ENST00000299084.8:c.33-146_33-144del	ENSP00000299084.4:n.33-146_33-144del
ENST00000561205.1:n.371-146_371-144del
ENST00000561317.1:c.-31-146_-31-144del	ENSP00000453680.1:n.-31-146_-31-144del
NM_152594.2:c.33-146_33-144del	NP_689807.1:n.33-146_33-144del
XM_005254202.2:c.69-146_69-144del	XP_005254259.1:n.69-146_69-144del
XM_005254203.3:c.-15-23014_-15-23012del	XP_005254260.1:n.-15-23014_-15-23012del
XM_011521288.1:c.-31-146_-31-144del	XP_011519590.1:n.-31-146_-31-144del
XM_011521289.1:c.-31-146_-31-144del	XP_011519591.1:n.-31-146_-31-144del
XM_011521290.1:c.-31-146_-31-144del	XP_011519592.1:n.-31-146_-31-144del
XM_005254202.3:c.69-146_69-144del	XP_005254259.1:n.69-146_69-144del
XM_011521289.3:c.-31-146_-31-144del	XP_011519591.1:n.-31-146_-31-144del
NM_152594.3:c.33-146_33-144del MANE Select	NP_689807.1:n.33-146_33-144del