Canonical Allele Identifier: CA2627714197
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38252989_38253011del , CM000677.2:g.38252989_38253011del GRCh38
NC_000015.9:g.38545190_38545212del , CM000677.1:g.38545190_38545212del GRCh37
NC_000015.8:g.36332482_36332504del NCBI36
NG_008980.1:g.5139_5161del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-197_-175del MANE Select ENSP00000299084.4:n.-197_-175del
ENST00000299084.8:c.-197_-175del ENSP00000299084.4:n.-197_-175del
ENST00000561205.1:n.142_164del
NM_152594.2:c.-197_-175del NP_689807.1:n.-197_-175del
XM_005254202.2:c.-197_-175del XP_005254259.1:n.-197_-175del
XM_005254203.3:c.-244_-222del XP_005254260.1:n.-244_-222del
XM_005254202.3:c.-197_-175del XP_005254259.1:n.-197_-175del
XR_001751484.1:n.87+560_87+582del
NM_152594.3:c.-197_-175del MANE Select NP_689807.1:n.-197_-175del