Canonical Allele Identifier: CA2170765652

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253060T= , CM000677.2:g.38253060T=	GRCh38
NC_000015.9:g.38545261T= , CM000677.1:g.38545261T=	GRCh37
NC_000015.8:g.36332553T=	NCBI36
NG_008980.1:g.5210T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.-126T= MANE Select	ENSP00000299084.4:n.-126T=
ENST00000299084.8:c.-126T=	ENSP00000299084.4:n.-126T=
ENST00000561205.1:n.213T=
NM_152594.2:c.-126T=	NP_689807.1:n.-126T=
XM_005254202.2:c.-126T=	XP_005254259.1:n.-126T=
XM_005254203.3:c.-173T=	XP_005254260.1:n.-173T=
XM_005254202.3:c.-126T=	XP_005254259.1:n.-126T=
XR_001751484.1:n.87+507A=
NM_152594.3:c.-126T= MANE Select	NP_689807.1:n.-126T=