Canonical Allele Identifier: CA2170812643

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351270A= , CM000677.2:g.38351270A=	GRCh38
NC_000015.9:g.38643471A= , CM000677.1:g.38643471A=	GRCh37
NC_000015.8:g.36430763A=	NCBI36
NG_008980.1:g.103420A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.941A= MANE Select	ENSP00000299084.4:p.Gln314=
ENST00000299084.8:c.941A=	ENSP00000299084.4:p.Gln314=
NM_152594.2:c.941A=	NP_689807.1:p.Gln314=
XM_005254202.2:c.977A=	XP_005254259.1:p.Gln326=
XM_005254203.3:c.719A=	XP_005254260.1:p.Gln240=
XM_011521288.1:c.878A=	XP_011519590.1:p.Gln293=
XM_011521289.1:c.878A=	XP_011519591.1:p.Gln293=
XM_011521290.1:c.878A=	XP_011519592.1:p.Gln293=
XM_005254202.3:c.977A=	XP_005254259.1:p.Gln326=
XM_011521289.3:c.878A=	XP_011519591.1:p.Gln293=
NM_152594.3:c.941A= MANE Select	NP_689807.1:p.Gln314=