Canonical Allele Identifier: CA2170812661

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351311G= , CM000677.2:g.38351311G=	GRCh38
NC_000015.9:g.38643512G= , CM000677.1:g.38643512G=	GRCh37
NC_000015.8:g.36430804G=	NCBI36
NG_008980.1:g.103461G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.982G= MANE Select	ENSP00000299084.4:p.Glu328=
ENST00000299084.8:c.982G=	ENSP00000299084.4:p.Glu328=
NM_152594.2:c.982G=	NP_689807.1:p.Glu328=
XM_005254202.2:c.1018G=	XP_005254259.1:p.Glu340=
XM_005254203.3:c.760G=	XP_005254260.1:p.Glu254=
XM_011521288.1:c.919G=	XP_011519590.1:p.Glu307=
XM_011521289.1:c.919G=	XP_011519591.1:p.Glu307=
XM_011521290.1:c.919G=	XP_011519592.1:p.Glu307=
XM_005254202.3:c.1018G=	XP_005254259.1:p.Glu340=
XM_011521289.3:c.919G=	XP_011519591.1:p.Glu307=
NM_152594.3:c.982G= MANE Select	NP_689807.1:p.Glu328=