Canonical Allele Identifier: CA2170765825

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253207T= , CM000677.2:g.38253207T=	GRCh38
NC_000015.9:g.38545408T= , CM000677.1:g.38545408T=	GRCh37
NC_000015.8:g.36332700T=	NCBI36
NG_008980.1:g.5357T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.22T= MANE Select	ENSP00000299084.4:p.Ser8=
ENST00000299084.8:c.22T=	ENSP00000299084.4:p.Ser8=
ENST00000561205.1:n.360T=
ENST00000561317.1:c.-106T=	ENSP00000453680.1:n.-106T=
NM_152594.2:c.22T=	NP_689807.1:p.Ser8=
XM_005254202.2:c.22T=	XP_005254259.1:p.Ser8=
XM_005254203.3:c.-26T=	XP_005254260.1:n.-26T=
XM_005254202.3:c.22T=	XP_005254259.1:p.Ser8=
XR_001751484.1:n.87+360A=
NM_152594.3:c.22T= MANE Select	NP_689807.1:p.Ser8=