Canonical Allele Identifier: CA2170788979

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299395G= , CM000677.2:g.38299395G=	GRCh38
NC_000015.9:g.38591596G= , CM000677.1:g.38591596G=	GRCh37
NC_000015.8:g.36378888G=	NCBI36
NG_008980.1:g.51545G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.55G= MANE Select	ENSP00000299084.4:p.Ala19=
ENST00000299084.8:c.55G=	ENSP00000299084.4:p.Ala19=
ENST00000561205.1:n.393G=
ENST00000561317.1:c.-9G=	ENSP00000453680.1:n.-9G=
NM_152594.2:c.55G=	NP_689807.1:p.Ala19=
XM_005254202.2:c.91G=	XP_005254259.1:p.Ala31=
XM_005254203.3:c.-15-22846G=	XP_005254260.1:n.-15-22846G=
XM_011521288.1:c.-9G=	XP_011519590.1:n.-9G=
XM_011521289.1:c.-9G=	XP_011519591.1:n.-9G=
XM_011521290.1:c.-9G=	XP_011519592.1:n.-9G=
XM_005254202.3:c.91G=	XP_005254259.1:p.Ala31=
XM_011521289.3:c.-9G=	XP_011519591.1:n.-9G=
NM_152594.3:c.55G= MANE Select	NP_689807.1:p.Ala19=