Canonical Allele Identifier: CA2170812780

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351607C= , CM000677.2:g.38351607C=	GRCh38
NC_000015.9:g.38643808C= , CM000677.1:g.38643808C=	GRCh37
NC_000015.8:g.36431100C=	NCBI36
NG_008980.1:g.103757C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1278C= MANE Select	ENSP00000299084.4:p.Cys426=
ENST00000299084.8:c.1278C=	ENSP00000299084.4:p.Cys426=
NM_152594.2:c.1278C=	NP_689807.1:p.Cys426=
XM_005254202.2:c.1314C=	XP_005254259.1:p.Cys438=
XM_005254203.3:c.1056C=	XP_005254260.1:p.Cys352=
XM_011521288.1:c.1215C=	XP_011519590.1:p.Cys405=
XM_011521289.1:c.1215C=	XP_011519591.1:p.Cys405=
XM_011521290.1:c.1215C=	XP_011519592.1:p.Cys405=
XM_005254202.3:c.1314C=	XP_005254259.1:p.Cys438=
XM_011521289.3:c.1215C=	XP_011519591.1:p.Cys405=
NM_152594.3:c.1278C= MANE Select	NP_689807.1:p.Cys426=