Canonical Allele Identifier: CA2170812902

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351854_38351860delinsGTTTTGT , CM000677.2:g.38351854_38351860delinsGTTTTGT	GRCh38
NC_000015.9:g.38644055_38644061delinsGTTTTGT , CM000677.1:g.38644055_38644061delinsGTTTTGT	GRCh37
NC_000015.8:g.36431347_36431353delinsGTTTTGT	NCBI36
NG_008980.1:g.104004_104010delinsGTTTTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*190_*196delinsGTTTTGT MANE Select	ENSP00000299084.4:n.*190_*196delinsGTTTTGT
ENST00000299084.8:c.*190_*196delinsGTTTTGT	ENSP00000299084.4:n.*190_*196delinsGTTTTGT
NM_152594.2:c.*190_*196delinsGTTTTGT	NP_689807.1:n.*190_*196delinsGTTTTGT
XM_005254202.2:c.*190_*196delinsGTTTTGT	XP_005254259.1:n.*190_*196delinsGTTTTGT
XM_005254203.3:c.*190_*196delinsGTTTTGT	XP_005254260.1:n.*190_*196delinsGTTTTGT
XM_011521288.1:c.*190_*196delinsGTTTTGT	XP_011519590.1:n.*190_*196delinsGTTTTGT
XM_011521289.1:c.*190_*196delinsGTTTTGT	XP_011519591.1:n.*190_*196delinsGTTTTGT
XM_011521290.1:c.*190_*196delinsGTTTTGT	XP_011519592.1:n.*190_*196delinsGTTTTGT
XM_005254202.3:c.*190_*196delinsGTTTTGT	XP_005254259.1:n.*190_*196delinsGTTTTGT
XM_011521289.3:c.*190_*196delinsGTTTTGT	XP_011519591.1:n.*190_*196delinsGTTTTGT
NM_152594.3:c.*190_*196delinsGTTTTGT MANE Select	NP_689807.1:n.*190_*196delinsGTTTTGT