Canonical Allele Identifier: CA658761229

Gene: SPRED1

Linked Data

• PubMed: PMID:19920235

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.38299400_38299401insC , CM000677.2:g.38299400_38299401insC	GRCh38
NC_000015.9:g.38591601_38591602insC , CM000677.1:g.38591601_38591602insC	GRCh37
NC_000015.8:g.36378893_36378894insC	NCBI36
NG_008980.1:g.51550_51551insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299084.9:c.60_61insC MANE Select	ENSP00000299084.4:p.Val21ArgfsTer6
ENST00000299084.8:c.60_61insC	ENSP00000299084.4:p.Val21ArgfsTer6
ENST00000561205.1:n.398_399insC
ENST00000561317.1:c.-4_-3insC	ENSP00000453680.1:n.-4_-3insC
NM_152594.2:c.60_61insC	NP_689807.1:p.Val21ArgfsTer6
XM_005254202.2:c.96_97insC	XP_005254259.1:p.Val33ArgfsTer6
XM_005254203.3:c.-15-22841_-15-22840insC	XP_005254260.1:n.-15-22841_-15-22840insC
XM_011521288.1:c.-4_-3insC	XP_011519590.1:n.-4_-3insC
XM_011521289.1:c.-4_-3insC	XP_011519591.1:n.-4_-3insC
XM_011521290.1:c.-4_-3insC	XP_011519592.1:n.-4_-3insC
XM_005254202.3:c.96_97insC	XP_005254259.1:p.Val33ArgfsTer6
XM_011521289.3:c.-4_-3insC	XP_011519591.1:n.-4_-3insC
NM_152594.3:c.60_61insC MANE Select	NP_689807.1:p.Val21ArgfsTer6