Canonical Allele Identifier: CA2170765854

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253217A= , CM000677.2:g.38253217A=	GRCh38
NC_000015.9:g.38545418A= , CM000677.1:g.38545418A=	GRCh37
NC_000015.8:g.36332710A=	NCBI36
NG_008980.1:g.5367A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.32A= MANE Select	ENSP00000299084.4:p.Asp11=
ENST00000299084.8:c.32A=	ENSP00000299084.4:p.Asp11=
ENST00000561205.1:n.370A=
ENST00000561317.1:c.-96A=	ENSP00000453680.1:n.-96A=
NM_152594.2:c.32A=	NP_689807.1:p.Asp11=
XM_005254202.2:c.32A=	XP_005254259.1:p.Glu11=
XM_005254203.3:c.-16A=	XP_005254260.1:n.-16A=
XM_005254202.3:c.32A=	XP_005254259.1:p.Glu11=
XR_001751484.1:n.87+350T=
NM_152594.3:c.32A= MANE Select	NP_689807.1:p.Asp11=