Canonical Allele Identifier: CA2170765566

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38252991_38252992delinsAC , CM000677.2:g.38252991_38252992delinsAC	GRCh38
NC_000015.9:g.38545192_38545193delinsAC , CM000677.1:g.38545192_38545193delinsAC	GRCh37
NC_000015.8:g.36332484_36332485delinsAC	NCBI36
NG_008980.1:g.5141_5142delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-195_-194delinsAC MANE Select	ENSP00000299084.4:n.-195_-194delinsAC
ENST00000299084.8:c.-195_-194delinsAC	ENSP00000299084.4:n.-195_-194delinsAC
ENST00000561205.1:n.144_145delinsAC
NM_152594.2:c.-195_-194delinsAC	NP_689807.1:n.-195_-194delinsAC
XM_005254202.2:c.-195_-194delinsAC	XP_005254259.1:n.-195_-194delinsAC
XM_005254203.3:c.-242_-241delinsAC	XP_005254260.1:n.-242_-241delinsAC
XM_005254202.3:c.-195_-194delinsAC	XP_005254259.1:n.-195_-194delinsAC
XR_001751484.1:n.87+575_87+576delinsGT
NM_152594.3:c.-195_-194delinsAC MANE Select	NP_689807.1:n.-195_-194delinsAC