Canonical Allele Identifier: CA2170812724

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351475C= , CM000677.2:g.38351475C=	GRCh38
NC_000015.9:g.38643676C= , CM000677.1:g.38643676C=	GRCh37
NC_000015.8:g.36430968C=	NCBI36
NG_008980.1:g.103625C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1146C= MANE Select	ENSP00000299084.4:p.Asp382=
ENST00000299084.8:c.1146C=	ENSP00000299084.4:p.Asp382=
NM_152594.2:c.1146C=	NP_689807.1:p.Asp382=
XM_005254202.2:c.1182C=	XP_005254259.1:p.Asp394=
XM_005254203.3:c.924C=	XP_005254260.1:p.Asp308=
XM_011521288.1:c.1083C=	XP_011519590.1:p.Asp361=
XM_011521289.1:c.1083C=	XP_011519591.1:p.Asp361=
XM_011521290.1:c.1083C=	XP_011519592.1:p.Asp361=
XM_005254202.3:c.1182C=	XP_005254259.1:p.Asp394=
XM_011521289.3:c.1083C=	XP_011519591.1:p.Asp361=
NM_152594.3:c.1146C= MANE Select	NP_689807.1:p.Asp382=