Canonical Allele Identifier: CA2170812545

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351017C= , CM000677.2:g.38351017C=	GRCh38
NC_000015.9:g.38643218C= , CM000677.1:g.38643218C=	GRCh37
NC_000015.8:g.36430510C=	NCBI36
NG_008980.1:g.103167C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000299084.9:c.688C= MANE Select	ENSP00000299084.4:p.Pro230=
ENST00000299084.8:c.688C=	ENSP00000299084.4:p.Pro230=
NM_152594.2:c.688C=	NP_689807.1:p.Pro230=
XM_005254202.2:c.724C=	XP_005254259.1:p.Pro242=
XM_005254203.3:c.466C=	XP_005254260.1:p.Pro156=
XM_011521288.1:c.625C=	XP_011519590.1:p.Pro209=
XM_011521289.1:c.625C=	XP_011519591.1:p.Pro209=
XM_011521290.1:c.625C=	XP_011519592.1:p.Pro209=
XM_005254202.3:c.724C=	XP_005254259.1:p.Pro242=
XM_011521289.3:c.625C=	XP_011519591.1:p.Pro209=
NM_152594.3:c.688C= MANE Select	NP_689807.1:p.Pro230=