Canonical Allele Identifier: CA16042989
Gene: SPRED1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 373025
ClinVar RCV Id: RCV000413626
dbSNP Id: rs1057518150
COSMIC: COSM168127

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38299411G>A , CM000677.2:g.38299411G>A GRCh38
NC_000015.9:g.38591612G>A , CM000677.1:g.38591612G>A GRCh37
NC_000015.8:g.36378904G>A NCBI36
NG_008980.1:g.51561G>A

Transcript Alleles

HGVS Amino-acid change
NM_152594.2:c.71G>A VV NP_689807.1:p.Arg24Gln
XM_005254202.2:c.107G>A XP_005254259.1:p.Arg36Gln
XM_005254203.3:c.-15-22830G>A XP_005254260.1:p.=
XM_011521288.1:c.8G>A XP_011519590.1:p.Arg3Gln
XM_011521289.1:c.8G>A XP_011519591.1:p.Arg3Gln
XM_011521290.1:c.8G>A XP_011519592.1:p.Arg3Gln
XM_005254202.3:c.107G>A XP_005254259.1:p.Arg36Gln
XM_011521289.3:c.8G>A XP_011519591.1:p.Arg3Gln
NM_152594.3:c.71G>A VV MANE Preferred NP_689807.1:p.Arg24Gln
ENST00000299084.8:c.71G>A ENSP00000299084.4:p.Arg24Gln
ENST00000561205.1:n.409G>A
ENST00000561317.1:c.8G>A ENSP00000453680.1:p.Arg3Gln