Canonical Allele Identifier: CA2838538504

Gene: SPRED1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351623dup , CM000677.2:g.38351623dup	GRCh38
NC_000015.9:g.38643824dup , CM000677.1:g.38643824dup	GRCh37
NC_000015.8:g.36431116dup	NCBI36
NG_008980.1:g.103773dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.1294dup MANE Select	ENSP00000299084.4:p.Ala432GlyfsTer10
ENST00000299084.8:c.1294dup	ENSP00000299084.4:p.Ala432GlyfsTer10
NM_152594.2:c.1294dup	NP_689807.1:p.Ala432GlyfsTer10
XM_005254202.2:c.1330dup	XP_005254259.1:p.Ala444GlyfsTer10
XM_005254203.3:c.1072dup	XP_005254260.1:p.Ala358GlyfsTer10
XM_011521288.1:c.1231dup	XP_011519590.1:p.Ala411GlyfsTer10
XM_011521289.1:c.1231dup	XP_011519591.1:p.Ala411GlyfsTer10
XM_011521290.1:c.1231dup	XP_011519592.1:p.Ala411GlyfsTer10
XM_005254202.3:c.1330dup	XP_005254259.1:p.Ala444GlyfsTer10
XM_011521289.3:c.1231dup	XP_011519591.1:p.Ala411GlyfsTer10
NM_152594.3:c.1294dup MANE Select	NP_689807.1:p.Ala432GlyfsTer10