Canonical Allele Identifier: CA1979439971
Gene: EFEMP2 HGNC NCBI
MUS81 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65867071G= , CM000673.2:g.65867071G= GRCh38
NC_000011.9:g.65634542G= , CM000673.1:g.65634542G= GRCh37
NC_000011.8:g.65391118G= NCBI36
NG_012304.2:g.10864C=
NG_053116.1:g.12010G=

Transcript Alleles

HGVS Amino-acid change
ENST00000307998.11:c.1179C= (EFEMP2) MANE Select ENSP00000309953.6:p.Asn393=
ENST00000307998.10:c.1179C= (EFEMP2) ENSP00000309953.6:p.Asn393=
ENST00000524408.1:c.55C= (EFEMP2)
ENST00000525006.1:n.38-186G= (MUS81)
ENST00000526628.5:n.1745C= (EFEMP2)
ENST00000526911.1:c.156C= (EFEMP2) ENSP00000436536.1:p.Asn52=
ENST00000527277.5:c.10C= (EFEMP2)
ENST00000528176.5:c.1171-359C= (EFEMP2) ENSP00000434151.1:n.1171-359C=
ENST00000528409.1:n.412C= (EFEMP2)
ENST00000530806.5:c.138C= (EFEMP2) ENSP00000436526.1:p.Asn46=
ENST00000531645.5:c.319-137C= (EFEMP2) ENSP00000436521.1:n.319-137C=
ENST00000531972.5:c.1179C= (EFEMP2) ENSP00000435295.1:p.Asn393=
ENST00000532648.1:n.34C= (EFEMP2)
NM_016938.4:c.1179C= (EFEMP2) NP_058634.4:p.Asn393=
NR_037718.1:n.1438C= (EFEMP2)
NR_146598.1:n.1845-186G= (MUS81)
NM_016938.5:c.1179C= (EFEMP2) MANE Select NP_058634.4:p.Asn393=
NR_037718.2:n.1304C= (EFEMP2)
NR_146598.2:n.1813-186G= (MUS81)