Canonical Allele Identifier: CA2170765819

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253202C= , CM000677.2:g.38253202C=	GRCh38
NC_000015.9:g.38545403C= , CM000677.1:g.38545403C=	GRCh37
NC_000015.8:g.36332695C=	NCBI36
NG_008980.1:g.5352C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.17C= MANE Select	ENSP00000299084.4:p.Ala6=
ENST00000299084.8:c.17C=	ENSP00000299084.4:p.Ala6=
ENST00000561205.1:n.355C=
ENST00000561317.1:c.-111C=	ENSP00000453680.1:n.-111C=
NM_152594.2:c.17C=	NP_689807.1:p.Ala6=
XM_005254202.2:c.17C=	XP_005254259.1:p.Ala6=
XM_005254203.3:c.-31C=	XP_005254260.1:n.-31C=
XM_005254202.3:c.17C=	XP_005254259.1:p.Ala6=
XR_001751484.1:n.87+365G=
NM_152594.3:c.17C= MANE Select	NP_689807.1:p.Ala6=