Canonical Allele Identifier: CA2170811834

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38349480G= , CM000677.2:g.38349480G=	GRCh38
NC_000015.9:g.38641681G= , CM000677.1:g.38641681G=	GRCh37
NC_000015.8:g.36428973G=	NCBI36
NG_008980.1:g.101630G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.641G= MANE Select	ENSP00000299084.4:p.Arg214=
ENST00000299084.8:c.641G=	ENSP00000299084.4:p.Arg214=
NM_152594.2:c.641G=	NP_689807.1:p.Arg214=
XM_005254202.2:c.677G=	XP_005254259.1:p.Arg226=
XM_005254203.3:c.419G=	XP_005254260.1:p.Arg140=
XM_011521288.1:c.578G=	XP_011519590.1:p.Arg193=
XM_011521289.1:c.578G=	XP_011519591.1:p.Arg193=
XM_011521290.1:c.578G=	XP_011519592.1:p.Arg193=
XM_005254202.3:c.677G=	XP_005254259.1:p.Arg226=
XM_011521289.3:c.578G=	XP_011519591.1:p.Arg193=
NM_152594.3:c.641G= MANE Select	NP_689807.1:p.Arg214=