Canonical Allele Identifier: CA2627714163

Gene: SPRED1

Linked Data

• gnomAD v4: 15-38252958-GCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38252959_38252960del , CM000677.2:g.38252959_38252960del	GRCh38
NC_000015.9:g.38545160_38545161del , CM000677.1:g.38545160_38545161del	GRCh37
NC_000015.8:g.36332452_36332453del	NCBI36
NG_008980.1:g.5109_5110del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-227_-226del MANE Select	ENSP00000299084.4:n.-227_-226del
ENST00000299084.8:c.-227_-226del	ENSP00000299084.4:n.-227_-226del
ENST00000561205.1:n.112_113del
NM_152594.2:c.-227_-226del	NP_689807.1:n.-227_-226del
XM_005254202.2:c.-227_-226del	XP_005254259.1:n.-227_-226del
XM_005254203.3:c.-274_-273del	XP_005254260.1:n.-274_-273del
XM_005254202.3:c.-227_-226del	XP_005254259.1:n.-227_-226del
XR_001751484.1:n.87+607_87+608del
NM_152594.3:c.-227_-226del MANE Select	NP_689807.1:n.-227_-226del