Canonical Allele Identifier: CA381349776
Gene: EFEMP2 HGNC NCBI
MUS81 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65867068G>C , CM000673.2:g.65867068G>C GRCh38
NC_000011.9:g.65634539G>C , CM000673.1:g.65634539G>C GRCh37
NC_000011.8:g.65391115G>C NCBI36
NG_012304.2:g.10867C>G
NG_053116.1:g.12007G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000307998.11:c.1182C>G (EFEMP2) MANE Select ENSP00000309953.6:p.Asn394Lys
ENST00000307998.10:c.1182C>G (EFEMP2) ENSP00000309953.6:p.Asn394Lys
ENST00000524408.1:c.58C>G (EFEMP2)
ENST00000525006.1:n.38-189G>C (MUS81)
ENST00000526628.5:n.1748C>G (EFEMP2)
ENST00000526911.1:c.159C>G (EFEMP2) ENSP00000436536.1:p.Asn53Lys
ENST00000527277.5:c.13C>G (EFEMP2)
ENST00000528176.5:c.1171-356C>G (EFEMP2) ENSP00000434151.1:n.1171-356C>G
ENST00000528409.1:n.415C>G (EFEMP2)
ENST00000530806.5:c.141C>G (EFEMP2) ENSP00000436526.1:p.Asn47Lys
ENST00000531645.5:c.319-134C>G (EFEMP2) ENSP00000436521.1:n.319-134C>G
ENST00000531972.5:c.1182C>G (EFEMP2) ENSP00000435295.1:p.Asn394Lys
ENST00000532648.1:n.37C>G (EFEMP2)
NM_016938.4:c.1182C>G (EFEMP2) NP_058634.4:p.Asn394Lys
NR_037718.1:n.1441C>G (EFEMP2)
NR_146598.1:n.1845-189G>C (MUS81)
NM_016938.5:c.1182C>G (EFEMP2) MANE Select NP_058634.4:p.Asn394Lys
NR_037718.2:n.1307C>G (EFEMP2)
NR_146598.2:n.1813-189G>C (MUS81)