Canonical Allele Identifier: CA2170765816

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253195G= , CM000677.2:g.38253195G=	GRCh38
NC_000015.9:g.38545396G= , CM000677.1:g.38545396G=	GRCh37
NC_000015.8:g.36332688G=	NCBI36
NG_008980.1:g.5345G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.10G= MANE Select	ENSP00000299084.4:p.Glu4=
ENST00000299084.8:c.10G=	ENSP00000299084.4:p.Glu4=
ENST00000561205.1:n.348G=
ENST00000561317.1:c.-118G=	ENSP00000453680.1:n.-118G=
NM_152594.2:c.10G=	NP_689807.1:p.Glu4=
XM_005254202.2:c.10G=	XP_005254259.1:p.Glu4=
XM_005254203.3:c.-38G=	XP_005254260.1:n.-38G=
XM_005254202.3:c.10G=	XP_005254259.1:p.Glu4=
XR_001751484.1:n.87+372C=
NM_152594.3:c.10G= MANE Select	NP_689807.1:p.Glu4=