Canonical Allele Identifier: CA391931803
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253192G>C , CM000677.2:g.38253192G>C GRCh38
NC_000015.9:g.38545393G>C , CM000677.1:g.38545393G>C GRCh37
NC_000015.8:g.36332685G>C NCBI36
NG_008980.1:g.5342G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.7G>C MANE Select ENSP00000299084.4:p.Glu3Gln
ENST00000299084.8:c.7G>C ENSP00000299084.4:p.Glu3Gln
ENST00000561205.1:n.345G>C
ENST00000561317.1:c.-121G>C ENSP00000453680.1:n.-121G>C
NM_152594.2:c.7G>C NP_689807.1:p.Glu3Gln
XM_005254202.2:c.7G>C XP_005254259.1:p.Glu3Gln
XM_005254203.3:c.-41G>C XP_005254260.1:n.-41G>C
XM_005254202.3:c.7G>C XP_005254259.1:p.Glu3Gln
XR_001751484.1:n.87+375C>G
NM_152594.3:c.7G>C MANE Select NP_689807.1:p.Glu3Gln