Canonical Allele Identifier: CA2170788967

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299379T= , CM000677.2:g.38299379T=	GRCh38
NC_000015.9:g.38591580T= , CM000677.1:g.38591580T=	GRCh37
NC_000015.8:g.36378872T=	NCBI36
NG_008980.1:g.51529T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.39T= MANE Select	ENSP00000299084.4:p.Ser13=
ENST00000299084.8:c.39T=	ENSP00000299084.4:p.Ser13=
ENST00000561205.1:n.377T=
ENST00000561317.1:c.-25T=	ENSP00000453680.1:n.-25T=
NM_152594.2:c.39T=	NP_689807.1:p.Ser13=
XM_005254202.2:c.75T=	XP_005254259.1:p.Ser25=
XM_005254203.3:c.-15-22862T=	XP_005254260.1:n.-15-22862T=
XM_011521288.1:c.-25T=	XP_011519590.1:n.-25T=
XM_011521289.1:c.-25T=	XP_011519591.1:n.-25T=
XM_011521290.1:c.-25T=	XP_011519592.1:n.-25T=
XM_005254202.3:c.75T=	XP_005254259.1:p.Ser25=
XM_011521289.3:c.-25T=	XP_011519591.1:n.-25T=
NM_152594.3:c.39T= MANE Select	NP_689807.1:p.Ser13=