Canonical Allele Identifier: CA2170812762

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351551G= , CM000677.2:g.38351551G=	GRCh38
NC_000015.9:g.38643752G= , CM000677.1:g.38643752G=	GRCh37
NC_000015.8:g.36431044G=	NCBI36
NG_008980.1:g.103701G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1222G= MANE Select	ENSP00000299084.4:p.Val408=
ENST00000299084.8:c.1222G=	ENSP00000299084.4:p.Val408=
NM_152594.2:c.1222G=	NP_689807.1:p.Val408=
XM_005254202.2:c.1258G=	XP_005254259.1:p.Val420=
XM_005254203.3:c.1000G=	XP_005254260.1:p.Val334=
XM_011521288.1:c.1159G=	XP_011519590.1:p.Val387=
XM_011521289.1:c.1159G=	XP_011519591.1:p.Val387=
XM_011521290.1:c.1159G=	XP_011519592.1:p.Val387=
XM_005254202.3:c.1258G=	XP_005254259.1:p.Val420=
XM_011521289.3:c.1159G=	XP_011519591.1:p.Val387=
NM_152594.3:c.1222G= MANE Select	NP_689807.1:p.Val408=