Canonical Allele Identifier: CA1979439924
Gene: EFEMP2 HGNC NCBI
MUS81 HGNC NCBI

Linked Data

ClinVar Variation Id: 1739625
ClinVar RCV Id: RCV002331962
dbSNP Id: rs1859863045

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65867058_65867084del , CM000673.2:g.65867058_65867084del GRCh38
NC_000011.9:g.65634529_65634555del , CM000673.1:g.65634529_65634555del GRCh37
NC_000011.8:g.65391105_65391131del NCBI36
NG_012304.2:g.10854_10880del
NG_053116.1:g.11997_12023del

Transcript Alleles

HGVS Amino-acid change
ENST00000307998.11:c.1171-2_1195del (EFEMP2)
ENST00000307998.10:c.1171-2_1195del (EFEMP2)
ENST00000524408.1:c.47-2_71del (EFEMP2)
ENST00000525006.1:n.38-199_38-173del (MUS81)
ENST00000526628.5:n.1737-2_1761del (EFEMP2)
ENST00000526911.1:c.148-2_172del (EFEMP2)
ENST00000528176.5:c.1171-369_1171-343del (EFEMP2) ENSP00000434151.1:n.1171-369_1171-343del
ENST00000528409.1:n.404-2_428del (EFEMP2)
ENST00000530806.5:c.130-2_154del (EFEMP2)
ENST00000531645.5:c.319-147_319-121del (EFEMP2) ENSP00000436521.1:n.319-147_319-121del
ENST00000531972.5:c.1171-2_1195del (EFEMP2)
ENST00000532648.1:n.26-2_50del (EFEMP2)
NM_016938.4:c.1171-2_1195del (EFEMP2)
NR_037718.1:n.1430-2_1454del (EFEMP2)
NR_146598.1:n.1845-199_1845-173del (MUS81)
NM_016938.5:c.1171-2_1195del (EFEMP2)
NR_037718.2:n.1296-2_1320del (EFEMP2)
NR_146598.2:n.1813-199_1813-173del (MUS81)