Canonical Allele Identifier: CA1979439553

Gene: EFEMP2 MUS81

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65866970C= , CM000673.2:g.65866970C=	GRCh38
NC_000011.9:g.65634441C= , CM000673.1:g.65634441C=	GRCh37
NC_000011.8:g.65391017C=	NCBI36
NG_012304.2:g.10965G=
NG_053116.1:g.11909C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000307998.11:c.1280G= (EFEMP2) MANE Select	ENSP00000309953.6:p.Arg427=
ENST00000307998.10:c.1280G= (EFEMP2)	ENSP00000309953.6:p.Arg427=
ENST00000524408.1:c.156G= (EFEMP2)
ENST00000525006.1:n.38-287C= (MUS81)
ENST00000526628.5:n.1846G= (EFEMP2)
ENST00000526911.1:c.206+51G= (EFEMP2)	ENSP00000436536.1:n.206+51G=
ENST00000527277.5:c.111G= (EFEMP2)
ENST00000528176.5:c.1171-258G= (EFEMP2)	ENSP00000434151.1:n.1171-258G=
ENST00000528409.1:n.513G= (EFEMP2)
ENST00000531645.5:c.319-36G= (EFEMP2)	ENSP00000436521.1:n.319-36G=
ENST00000531972.5:c.1280G= (EFEMP2)	ENSP00000435295.1:p.Arg427=
ENST00000532648.1:n.135G= (EFEMP2)
NM_016938.4:c.1280G= (EFEMP2)	NP_058634.4:p.Arg427=
NR_037718.1:n.1539G= (EFEMP2)
NR_146598.1:n.1845-287C= (MUS81)
NM_016938.5:c.1280G= (EFEMP2) MANE Select	NP_058634.4:p.Arg427=
NR_037718.2:n.1405G= (EFEMP2)
NR_146598.2:n.1813-287C= (MUS81)