Canonical Allele Identifier: CA2170812668

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351318G= , CM000677.2:g.38351318G=	GRCh38
NC_000015.9:g.38643519G= , CM000677.1:g.38643519G=	GRCh37
NC_000015.8:g.36430811G=	NCBI36
NG_008980.1:g.103468G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.989G= MANE Select	ENSP00000299084.4:p.Gly330=
ENST00000299084.8:c.989G=	ENSP00000299084.4:p.Gly330=
NM_152594.2:c.989G=	NP_689807.1:p.Gly330=
XM_005254202.2:c.1025G=	XP_005254259.1:p.Gly342=
XM_005254203.3:c.767G=	XP_005254260.1:p.Gly256=
XM_011521288.1:c.926G=	XP_011519590.1:p.Gly309=
XM_011521289.1:c.926G=	XP_011519591.1:p.Gly309=
XM_011521290.1:c.926G=	XP_011519592.1:p.Gly309=
XM_005254202.3:c.1025G=	XP_005254259.1:p.Gly342=
XM_011521289.3:c.926G=	XP_011519591.1:p.Gly309=
NM_152594.3:c.989G= MANE Select	NP_689807.1:p.Gly330=