Canonical Allele Identifier: CA2627715130

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38299266-TCAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299270_38299272del , CM000677.2:g.38299270_38299272del	GRCh38
NC_000015.9:g.38591471_38591473del , CM000677.1:g.38591471_38591473del	GRCh37
NC_000015.8:g.36378763_36378765del	NCBI36
NG_008980.1:g.51420_51422del

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.33-103_33-101del MANE Select	ENSP00000299084.4:n.33-103_33-101del
ENST00000299084.8:c.33-103_33-101del	ENSP00000299084.4:n.33-103_33-101del
ENST00000561205.1:n.371-103_371-101del
ENST00000561317.1:c.-31-103_-31-101del	ENSP00000453680.1:n.-31-103_-31-101del
NM_152594.2:c.33-103_33-101del	NP_689807.1:n.33-103_33-101del
XM_005254202.2:c.69-103_69-101del	XP_005254259.1:n.69-103_69-101del
XM_005254203.3:c.-15-22971_-15-22969del	XP_005254260.1:n.-15-22971_-15-22969del
XM_011521288.1:c.-31-103_-31-101del	XP_011519590.1:n.-31-103_-31-101del
XM_011521289.1:c.-31-103_-31-101del	XP_011519591.1:n.-31-103_-31-101del
XM_011521290.1:c.-31-103_-31-101del	XP_011519592.1:n.-31-103_-31-101del
XM_005254202.3:c.69-103_69-101del	XP_005254259.1:n.69-103_69-101del
XM_011521289.3:c.-31-103_-31-101del	XP_011519591.1:n.-31-103_-31-101del
NM_152594.3:c.33-103_33-101del MANE Select	NP_689807.1:n.33-103_33-101del