Canonical Allele Identifier: CA2832566039

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38322117_38322120del , CM000677.2:g.38322117_38322120del	GRCh38
NC_000015.9:g.38614318_38614321del , CM000677.1:g.38614318_38614321del	GRCh37
NC_000015.8:g.36401610_36401613del	NCBI36
NG_008980.1:g.74267_74270del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.208-124_208-121del MANE Select	ENSP00000299084.4:n.208-124_208-121del
ENST00000299084.8:c.208-124_208-121del	ENSP00000299084.4:n.208-124_208-121del
ENST00000561205.1:n.546-124_546-121del
ENST00000561317.1:c.145-124_145-121del	ENSP00000453680.1:n.145-124_145-121del
NM_152594.2:c.208-124_208-121del	NP_689807.1:n.208-124_208-121del
XM_005254202.2:c.244-124_244-121del	XP_005254259.1:n.244-124_244-121del
XM_005254203.3:c.-15-124_-15-121del	XP_005254260.1:n.-15-124_-15-121del
XM_011521288.1:c.145-124_145-121del	XP_011519590.1:n.145-124_145-121del
XM_011521289.1:c.145-124_145-121del	XP_011519591.1:n.145-124_145-121del
XM_011521290.1:c.145-124_145-121del	XP_011519592.1:n.145-124_145-121del
XM_005254202.3:c.244-124_244-121del	XP_005254259.1:n.244-124_244-121del
XM_011521289.3:c.145-124_145-121del	XP_011519591.1:n.145-124_145-121del
NM_152594.3:c.208-124_208-121del MANE Select	NP_689807.1:n.208-124_208-121del