Canonical Allele Identifier: CA2170789081

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299661T= , CM000677.2:g.38299661T=	GRCh38
NC_000015.9:g.38591862T= , CM000677.1:g.38591862T=	GRCh37
NC_000015.8:g.36379154T=	NCBI36
NG_008980.1:g.51811T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.207+114T= MANE Select	ENSP00000299084.4:n.207+114T=
ENST00000299084.8:c.207+114T=	ENSP00000299084.4:n.207+114T=
ENST00000561205.1:n.545+114T=
ENST00000561317.1:c.144+114T=	ENSP00000453680.1:n.144+114T=
NM_152594.2:c.207+114T=	NP_689807.1:n.207+114T=
XM_005254202.2:c.243+114T=	XP_005254259.1:n.243+114T=
XM_005254203.3:c.-15-22580T=	XP_005254260.1:n.-15-22580T=
XM_011521288.1:c.144+114T=	XP_011519590.1:n.144+114T=
XM_011521289.1:c.144+114T=	XP_011519591.1:n.144+114T=
XM_011521290.1:c.144+114T=	XP_011519592.1:n.144+114T=
XM_005254202.3:c.243+114T=	XP_005254259.1:n.243+114T=
XM_011521289.3:c.144+114T=	XP_011519591.1:n.144+114T=
NM_152594.3:c.207+114T= MANE Select	NP_689807.1:n.207+114T=