Canonical Allele Identifier: CA391931808
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253194G>C , CM000677.2:g.38253194G>C GRCh38
NC_000015.9:g.38545395G>C , CM000677.1:g.38545395G>C GRCh37
NC_000015.8:g.36332687G>C NCBI36
NG_008980.1:g.5344G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.9G>C MANE Select ENSP00000299084.4:p.Glu3Asp
ENST00000299084.8:c.9G>C ENSP00000299084.4:p.Glu3Asp
ENST00000561205.1:n.347G>C
ENST00000561317.1:c.-119G>C ENSP00000453680.1:n.-119G>C
NM_152594.2:c.9G>C NP_689807.1:p.Glu3Asp
XM_005254202.2:c.9G>C XP_005254259.1:p.Glu3Asp
XM_005254203.3:c.-39G>C XP_005254260.1:n.-39G>C
XM_005254202.3:c.9G>C XP_005254259.1:p.Glu3Asp
XR_001751484.1:n.87+373C>G
NM_152594.3:c.9G>C MANE Select NP_689807.1:p.Glu3Asp