Canonical Allele Identifier: CA2170812586

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351137G= , CM000677.2:g.38351137G=	GRCh38
NC_000015.9:g.38643338G= , CM000677.1:g.38643338G=	GRCh37
NC_000015.8:g.36430630G=	NCBI36
NG_008980.1:g.103287G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.808G= MANE Select	ENSP00000299084.4:p.Asp270=
ENST00000299084.8:c.808G=	ENSP00000299084.4:p.Asp270=
NM_152594.2:c.808G=	NP_689807.1:p.Asp270=
XM_005254202.2:c.844G=	XP_005254259.1:p.Asp282=
XM_005254203.3:c.586G=	XP_005254260.1:p.Asp196=
XM_011521288.1:c.745G=	XP_011519590.1:p.Asp249=
XM_011521289.1:c.745G=	XP_011519591.1:p.Asp249=
XM_011521290.1:c.745G=	XP_011519592.1:p.Asp249=
XM_005254202.3:c.844G=	XP_005254259.1:p.Asp282=
XM_011521289.3:c.745G=	XP_011519591.1:p.Asp249=
NM_152594.3:c.808G= MANE Select	NP_689807.1:p.Asp270=