Canonical Allele Identifier: CA2170789123

Gene: SPRED1

Linked Data

• dbSNP Id: rs1895115958

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299745dup , CM000677.2:g.38299745dup	GRCh38
NC_000015.9:g.38591946dup , CM000677.1:g.38591946dup	GRCh37
NC_000015.8:g.36379238dup	NCBI36
NG_008980.1:g.51895dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.207+198dup MANE Select	ENSP00000299084.4:n.207+198dup
ENST00000299084.8:c.207+198dup	ENSP00000299084.4:n.207+198dup
ENST00000561205.1:n.545+198dup
ENST00000561317.1:c.144+198dup	ENSP00000453680.1:n.144+198dup
NM_152594.2:c.207+198dup	NP_689807.1:n.207+198dup
XM_005254202.2:c.243+198dup	XP_005254259.1:n.243+198dup
XM_005254203.3:c.-15-22496dup	XP_005254260.1:n.-15-22496dup
XM_011521288.1:c.144+198dup	XP_011519590.1:n.144+198dup
XM_011521289.1:c.144+198dup	XP_011519591.1:n.144+198dup
XM_011521290.1:c.144+198dup	XP_011519592.1:n.144+198dup
XM_005254202.3:c.243+198dup	XP_005254259.1:n.243+198dup
XM_011521289.3:c.144+198dup	XP_011519591.1:n.144+198dup
NM_152594.3:c.207+198dup MANE Select	NP_689807.1:n.207+198dup