Canonical Allele Identifier: CA391931839
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.23C>A MANE Select ENSP00000299084.4:p.Ser8Tyr
ENST00000299084.8:c.23C>A ENSP00000299084.4:p.Ser8Tyr
ENST00000561205.1:n.361C>A
ENST00000561317.1:c.-105C>A ENSP00000453680.1:n.-105C>A
NM_152594.2:c.23C>A NP_689807.1:p.Ser8Tyr
XM_005254202.2:c.23C>A XP_005254259.1:p.Ser8Tyr
XM_005254203.3:c.-25C>A XP_005254260.1:n.-25C>A
XM_005254202.3:c.23C>A XP_005254259.1:p.Ser8Tyr
XR_001751484.1:n.87+359G>T
NM_152594.3:c.23C>A MANE Select NP_689807.1:p.Ser8Tyr