Canonical Allele Identifier: CA2170765469

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38252891_38252893delinsCCT , CM000677.2:g.38252891_38252893delinsCCT	GRCh38
NC_000015.9:g.38545092_38545094delinsCCT , CM000677.1:g.38545092_38545094delinsCCT	GRCh37
NC_000015.8:g.36332384_36332386delinsCCT	NCBI36
NG_008980.1:g.5041_5043delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-295_-293delinsCCT MANE Select	ENSP00000299084.4:n.-295_-293delinsCCT
ENST00000299084.8:c.-295_-293delinsCCT	ENSP00000299084.4:n.-295_-293delinsCCT
ENST00000561205.1:n.44_46delinsCCT
NM_152594.2:c.-295_-293delinsCCT	NP_689807.1:n.-295_-293delinsCCT
XM_005254202.2:c.-295_-293delinsCCT	XP_005254259.1:n.-295_-293delinsCCT
XM_005254203.3:c.-342_-340delinsCCT	XP_005254260.1:n.-342_-340delinsCCT
XM_005254202.3:c.-295_-293delinsCCT	XP_005254259.1:n.-295_-293delinsCCT
XR_001751484.1:n.87+674_87+676delinsAGG
NM_152594.3:c.-295_-293delinsCCT MANE Select	NP_689807.1:n.-295_-293delinsCCT