Canonical Allele Identifier: CA2170765702
Gene: SPRED1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253107T= , CM000677.2:g.38253107T= GRCh38
NC_000015.9:g.38545308T= , CM000677.1:g.38545308T= GRCh37
NC_000015.8:g.36332600T= NCBI36
NG_008980.1:g.5257T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-79T= MANE Select ENSP00000299084.4:n.-79T=
ENST00000299084.8:c.-79T= ENSP00000299084.4:n.-79T=
ENST00000561205.1:n.260T=
NM_152594.2:c.-79T= NP_689807.1:n.-79T=
XM_005254202.2:c.-79T= XP_005254259.1:n.-79T=
XM_005254203.3:c.-126T= XP_005254260.1:n.-126T=
XM_005254202.3:c.-79T= XP_005254259.1:n.-79T=
XR_001751484.1:n.87+460A=
NM_152594.3:c.-79T= MANE Select NP_689807.1:n.-79T=
Search 100 bp 5'
Search 100 bp 3'