Canonical Allele Identifier: CA2627714225
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38253007_38253015del , CM000677.2:g.38253007_38253015del GRCh38
NC_000015.9:g.38545208_38545216del , CM000677.1:g.38545208_38545216del GRCh37
NC_000015.8:g.36332500_36332508del NCBI36
NG_008980.1:g.5157_5165del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.-179_-171del MANE Select ENSP00000299084.4:n.-179_-171del
ENST00000299084.8:c.-179_-171del ENSP00000299084.4:n.-179_-171del
ENST00000561205.1:n.160_168del
NM_152594.2:c.-179_-171del NP_689807.1:n.-179_-171del
XM_005254202.2:c.-179_-171del XP_005254259.1:n.-179_-171del
XM_005254203.3:c.-226_-218del XP_005254260.1:n.-226_-218del
XM_005254202.3:c.-179_-171del XP_005254259.1:n.-179_-171del
XR_001751484.1:n.87+557_87+565del
NM_152594.3:c.-179_-171del MANE Select NP_689807.1:n.-179_-171del