Canonical Allele Identifier: CA2170812655

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351302C= , CM000677.2:g.38351302C=	GRCh38
NC_000015.9:g.38643503C= , CM000677.1:g.38643503C=	GRCh37
NC_000015.8:g.36430795C=	NCBI36
NG_008980.1:g.103452C=

Transcript Alleles

HGVS	Amino-acid Change
NM_152594.3:c.973C= MANE Select	NP_689807.1:p.Arg325=
ENST00000299084.9:c.973C= MANE Select	ENSP00000299084.4:p.Arg325=
NM_152594.2:c.973C=	NP_689807.1:p.Arg325=
ENST00000299084.8:c.973C=	ENSP00000299084.4:p.Arg325=
XM_005254202.2:c.1009C=	XP_005254259.1:p.Arg337=
XM_005254202.3:c.1009C=	XP_005254259.1:p.Arg337=
XM_005254203.3:c.751C=	XP_005254260.1:p.Arg251=
XM_011521288.1:c.910C=	XP_011519590.1:p.Arg304=
XM_011521289.1:c.910C=	XP_011519591.1:p.Arg304=
XM_011521289.3:c.910C=	XP_011519591.1:p.Arg304=
XM_011521290.1:c.910C=	XP_011519592.1:p.Arg304=