Canonical Allele Identifier: CA2170765817

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253200G= , CM000677.2:g.38253200G=	GRCh38
NC_000015.9:g.38545401G= , CM000677.1:g.38545401G=	GRCh37
NC_000015.8:g.36332693G=	NCBI36
NG_008980.1:g.5350G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.15G= MANE Select	ENSP00000299084.4:p.Thr5=
ENST00000299084.8:c.15G=	ENSP00000299084.4:p.Thr5=
ENST00000561205.1:n.353G=
ENST00000561317.1:c.-113G=	ENSP00000453680.1:n.-113G=
NM_152594.2:c.15G=	NP_689807.1:p.Thr5=
XM_005254202.2:c.15G=	XP_005254259.1:p.Thr5=
XM_005254203.3:c.-33G=	XP_005254260.1:n.-33G=
XM_005254202.3:c.15G=	XP_005254259.1:p.Thr5=
XR_001751484.1:n.87+367C=
NM_152594.3:c.15G= MANE Select	NP_689807.1:p.Thr5=