Canonical Allele Identifier: CA2170789173

Gene: SPRED1

Linked Data

• dbSNP Id: rs1895118175

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299851dup , CM000677.2:g.38299851dup	GRCh38
NC_000015.9:g.38592052dup , CM000677.1:g.38592052dup	GRCh37
NC_000015.8:g.36379344dup	NCBI36
NG_008980.1:g.52001dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.207+304dup MANE Select	ENSP00000299084.4:n.207+304dup
ENST00000299084.8:c.207+304dup	ENSP00000299084.4:n.207+304dup
ENST00000561205.1:n.545+304dup
ENST00000561317.1:c.144+304dup	ENSP00000453680.1:n.144+304dup
NM_152594.2:c.207+304dup	NP_689807.1:n.207+304dup
XM_005254202.2:c.243+304dup	XP_005254259.1:n.243+304dup
XM_005254203.3:c.-15-22390dup	XP_005254260.1:n.-15-22390dup
XM_011521288.1:c.144+304dup	XP_011519590.1:n.144+304dup
XM_011521289.1:c.144+304dup	XP_011519591.1:n.144+304dup
XM_011521290.1:c.144+304dup	XP_011519592.1:n.144+304dup
XM_005254202.3:c.243+304dup	XP_005254259.1:n.243+304dup
XM_011521289.3:c.144+304dup	XP_011519591.1:n.144+304dup
NM_152594.3:c.207+304dup MANE Select	NP_689807.1:n.207+304dup