Canonical Allele Identifier: CA2170812887

Gene: SPRED1

Linked Data

• dbSNP Id: rs1888496867

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38351835dup , CM000677.2:g.38351835dup	GRCh38
NC_000015.9:g.38644036dup , CM000677.1:g.38644036dup	GRCh37
NC_000015.8:g.36431328dup	NCBI36
NG_008980.1:g.103985dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.*171dup MANE Select	ENSP00000299084.4:n.*171dup
ENST00000299084.8:c.*171dup	ENSP00000299084.4:n.*171dup
NM_152594.2:c.*171dup	NP_689807.1:n.*171dup
XM_005254202.2:c.*171dup	XP_005254259.1:n.*171dup
XM_005254203.3:c.*171dup	XP_005254260.1:n.*171dup
XM_011521288.1:c.*171dup	XP_011519590.1:n.*171dup
XM_011521289.1:c.*171dup	XP_011519591.1:n.*171dup
XM_011521290.1:c.*171dup	XP_011519592.1:n.*171dup
XM_005254202.3:c.*171dup	XP_005254259.1:n.*171dup
XM_011521289.3:c.*171dup	XP_011519591.1:n.*171dup
NM_152594.3:c.*171dup MANE Select	NP_689807.1:n.*171dup