Canonical Allele Identifier: CA391931840
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253208C>G , CM000677.2:g.38253208C>G GRCh38
NC_000015.9:g.38545409C>G , CM000677.1:g.38545409C>G GRCh37
NC_000015.8:g.36332701C>G NCBI36
NG_008980.1:g.5358C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.23C>G MANE Select ENSP00000299084.4:p.Ser8Cys
ENST00000299084.8:c.23C>G ENSP00000299084.4:p.Ser8Cys
ENST00000561205.1:n.361C>G
ENST00000561317.1:c.-105C>G ENSP00000453680.1:n.-105C>G
NM_152594.2:c.23C>G NP_689807.1:p.Ser8Cys
XM_005254202.2:c.23C>G XP_005254259.1:p.Ser8Cys
XM_005254203.3:c.-25C>G XP_005254260.1:n.-25C>G
XM_005254202.3:c.23C>G XP_005254259.1:p.Ser8Cys
XR_001751484.1:n.87+359G>C
NM_152594.3:c.23C>G MANE Select NP_689807.1:p.Ser8Cys