Canonical Allele Identifier: CA968819753
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38356436_38356439del , CM000677.2:g.38356436_38356439del GRCh38
NC_000015.9:g.38648637_38648640del , CM000677.1:g.38648637_38648640del GRCh37
NC_000015.8:g.36435929_36435932del NCBI36
NG_008980.1:g.108586_108589del

Transcript Alleles

HGVS Amino-acid change
ENST00000299084.9:c.*4772_*4775del MANE Select ENSP00000299084.4:n.*4772_*4775del
ENST00000299084.8:c.*4772_*4775del ENSP00000299084.4:n.*4772_*4775del
NM_152594.2:c.*4772_*4775del NP_689807.1:n.*4772_*4775del
XM_005254202.2:c.*4772_*4775del XP_005254259.1:n.*4772_*4775del
XM_005254203.3:c.*4772_*4775del XP_005254260.1:n.*4772_*4775del
XM_011521288.1:c.*4772_*4775del XP_011519590.1:n.*4772_*4775del
XM_011521289.1:c.*4772_*4775del XP_011519591.1:n.*4772_*4775del
XM_011521290.1:c.*4772_*4775del XP_011519592.1:n.*4772_*4775del
XM_005254202.3:c.*4772_*4775del XP_005254259.1:n.*4772_*4775del
XM_011521289.3:c.*4772_*4775del XP_011519591.1:n.*4772_*4775del
NM_152594.3:c.*4772_*4775del MANE Select NP_689807.1:n.*4772_*4775del