Canonical Allele Identifier: CA2627716207
Gene: SPRED1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.38351309_38351310del , CM000677.2:g.38351309_38351310del GRCh38
NC_000015.9:g.38643510_38643511del , CM000677.1:g.38643510_38643511del GRCh37
NC_000015.8:g.36430802_36430803del NCBI36
NG_008980.1:g.103459_103460del

Transcript Alleles

HGVS Amino-acid Change
ENST00000299084.9:c.980_981del MANE Select ENSP00000299084.4:p.Lys327ArgfsTer4
ENST00000299084.8:c.980_981del ENSP00000299084.4:p.Lys327ArgfsTer4
NM_152594.2:c.980_981del NP_689807.1:p.Lys327ArgfsTer4
XM_005254202.2:c.1016_1017del XP_005254259.1:p.Lys339ArgfsTer4
XM_005254203.3:c.758_759del XP_005254260.1:p.Lys253ArgfsTer4
XM_011521288.1:c.917_918del XP_011519590.1:p.Lys306ArgfsTer4
XM_011521289.1:c.917_918del XP_011519591.1:p.Lys306ArgfsTer4
XM_011521290.1:c.917_918del XP_011519592.1:p.Lys306ArgfsTer4
XM_005254202.3:c.1016_1017del XP_005254259.1:p.Lys339ArgfsTer4
XM_011521289.3:c.917_918del XP_011519591.1:p.Lys306ArgfsTer4
NM_152594.3:c.980_981del MANE Select NP_689807.1:p.Lys327ArgfsTer4