Canonical Allele Identifier: CA381349826
Gene: EFEMP2 HGNC NCBI
MUS81 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65867072T>A , CM000673.2:g.65867072T>A GRCh38
NC_000011.9:g.65634543T>A , CM000673.1:g.65634543T>A GRCh37
NC_000011.8:g.65391119T>A NCBI36
NG_012304.2:g.10863A>T
NG_053116.1:g.12011T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307998.11:c.1178A>T (EFEMP2) MANE Select ENSP00000309953.6:p.Asn393Ile
ENST00000307998.10:c.1178A>T (EFEMP2) ENSP00000309953.6:p.Asn393Ile
ENST00000524408.1:c.54A>T (EFEMP2)
ENST00000525006.1:n.38-185T>A (MUS81)
ENST00000526628.5:n.1744A>T (EFEMP2)
ENST00000526911.1:c.155A>T (EFEMP2) ENSP00000436536.1:p.Asn52Ile
ENST00000527277.5:c.9A>T (EFEMP2)
ENST00000528176.5:c.1171-360A>T (EFEMP2) ENSP00000434151.1:n.1171-360A>T
ENST00000528409.1:n.411A>T (EFEMP2)
ENST00000530806.5:c.137A>T (EFEMP2) ENSP00000436526.1:p.Asn46Ile
ENST00000531645.5:c.319-138A>T (EFEMP2) ENSP00000436521.1:n.319-138A>T
ENST00000531972.5:c.1178A>T (EFEMP2) ENSP00000435295.1:p.Asn393Ile
ENST00000532648.1:n.33A>T (EFEMP2)
NM_016938.4:c.1178A>T (EFEMP2) NP_058634.4:p.Asn393Ile
NR_037718.1:n.1437A>T (EFEMP2)
NR_146598.1:n.1845-185T>A (MUS81)
NM_016938.5:c.1178A>T (EFEMP2) MANE Select NP_058634.4:p.Asn393Ile
NR_037718.2:n.1303A>T (EFEMP2)
NR_146598.2:n.1813-185T>A (MUS81)