Canonical Allele Identifier: CA2841195946

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299329_38299330del , CM000677.2:g.38299329_38299330del	GRCh38
NC_000015.9:g.38591530_38591531del , CM000677.1:g.38591530_38591531del	GRCh37
NC_000015.8:g.36378822_36378823del	NCBI36
NG_008980.1:g.51479_51480del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.33-44_33-43del MANE Select	ENSP00000299084.4:n.33-44_33-43del
ENST00000299084.8:c.33-44_33-43del	ENSP00000299084.4:n.33-44_33-43del
ENST00000561205.1:n.371-44_371-43del
ENST00000561317.1:c.-31-44_-31-43del	ENSP00000453680.1:n.-31-44_-31-43del
NM_152594.2:c.33-44_33-43del	NP_689807.1:n.33-44_33-43del
XM_005254202.2:c.69-44_69-43del	XP_005254259.1:n.69-44_69-43del
XM_005254203.3:c.-15-22912_-15-22911del	XP_005254260.1:n.-15-22912_-15-22911del
XM_011521288.1:c.-31-44_-31-43del	XP_011519590.1:n.-31-44_-31-43del
XM_011521289.1:c.-31-44_-31-43del	XP_011519591.1:n.-31-44_-31-43del
XM_011521290.1:c.-31-44_-31-43del	XP_011519592.1:n.-31-44_-31-43del
XM_005254202.3:c.69-44_69-43del	XP_005254259.1:n.69-44_69-43del
XM_011521289.3:c.-31-44_-31-43del	XP_011519591.1:n.-31-44_-31-43del
NM_152594.3:c.33-44_33-43del MANE Select	NP_689807.1:n.33-44_33-43del