Canonical Allele Identifier: CA2170765828

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253208_38253209delinsCT , CM000677.2:g.38253208_38253209delinsCT	GRCh38
NC_000015.9:g.38545409_38545410delinsCT , CM000677.1:g.38545409_38545410delinsCT	GRCh37
NC_000015.8:g.36332701_36332702delinsCT	NCBI36
NG_008980.1:g.5358_5359delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.23_24delinsCT MANE Select	ENSP00000299084.4:p.Ser8=
ENST00000299084.8:c.23_24delinsCT	ENSP00000299084.4:p.Ser8=
ENST00000561205.1:n.361_362delinsCT
ENST00000561317.1:c.-105_-104delinsCT	ENSP00000453680.1:n.-105_-104delinsCT
NM_152594.2:c.23_24delinsCT	NP_689807.1:p.Ser8=
XM_005254202.2:c.23_24delinsCT	XP_005254259.1:p.Ser8=
XM_005254203.3:c.-25_-24delinsCT	XP_005254260.1:n.-25_-24delinsCT
XM_005254202.3:c.23_24delinsCT	XP_005254259.1:p.Ser8=
XR_001751484.1:n.87+358_87+359delinsAG
NM_152594.3:c.23_24delinsCT MANE Select	NP_689807.1:p.Ser8=