Canonical Allele Identifier: CA2170812619

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351217T= , CM000677.2:g.38351217T=	GRCh38
NC_000015.9:g.38643418T= , CM000677.1:g.38643418T=	GRCh37
NC_000015.8:g.36430710T=	NCBI36
NG_008980.1:g.103367T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.888T= MANE Select	ENSP00000299084.4:p.Cys296=
ENST00000299084.8:c.888T=	ENSP00000299084.4:p.Cys296=
NM_152594.2:c.888T=	NP_689807.1:p.Cys296=
XM_005254202.2:c.924T=	XP_005254259.1:p.Cys308=
XM_005254203.3:c.666T=	XP_005254260.1:p.Cys222=
XM_011521288.1:c.825T=	XP_011519590.1:p.Cys275=
XM_011521289.1:c.825T=	XP_011519591.1:p.Cys275=
XM_011521290.1:c.825T=	XP_011519592.1:p.Cys275=
XM_005254202.3:c.924T=	XP_005254259.1:p.Cys308=
XM_011521289.3:c.825T=	XP_011519591.1:p.Cys275=
NM_152594.3:c.888T= MANE Select	NP_689807.1:p.Cys296=