Canonical Allele Identifier: CA2170765951

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38253284C= , CM000677.2:g.38253284C=	GRCh38
NC_000015.9:g.38545485C= , CM000677.1:g.38545485C=	GRCh37
NC_000015.8:g.36332777C=	NCBI36
NG_008980.1:g.5434C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.32+67C= MANE Select	ENSP00000299084.4:n.32+67C=
ENST00000299084.8:c.32+67C=	ENSP00000299084.4:n.32+67C=
ENST00000561205.1:n.370+67C=
ENST00000561317.1:c.-96+67C=	ENSP00000453680.1:n.-96+67C=
NM_152594.2:c.32+67C=	NP_689807.1:n.32+67C=
XM_005254202.2:c.32+67C=	XP_005254259.1:n.32+67C=
XM_005254203.3:c.-16+67C=	XP_005254260.1:n.-16+67C=
XM_005254202.3:c.32+67C=	XP_005254259.1:n.32+67C=
XR_001751484.1:n.87+283G=
NM_152594.3:c.32+67C= MANE Select	NP_689807.1:n.32+67C=