Canonical Allele Identifier: CA2170765746

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253152C= , CM000677.2:g.38253152C=	GRCh38
NC_000015.9:g.38545353C= , CM000677.1:g.38545353C=	GRCh37
NC_000015.8:g.36332645C=	NCBI36
NG_008980.1:g.5302C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.-34C= MANE Select	ENSP00000299084.4:n.-34C=
ENST00000299084.8:c.-34C=	ENSP00000299084.4:n.-34C=
ENST00000561205.1:n.305C=
NM_152594.2:c.-34C=	NP_689807.1:n.-34C=
XM_005254202.2:c.-34C=	XP_005254259.1:n.-34C=
XM_005254203.3:c.-81C=	XP_005254260.1:n.-81C=
XM_005254202.3:c.-34C=	XP_005254259.1:n.-34C=
XR_001751484.1:n.87+415G=
NM_152594.3:c.-34C= MANE Select	NP_689807.1:n.-34C=