Canonical Allele Identifier: CA1979443908

Gene: EFEMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868338C= , CM000673.2:g.65868338C=	GRCh38
NC_000011.9:g.65635809C= , CM000673.1:g.65635809C=	GRCh37
NC_000011.8:g.65392385C=	NCBI36
NG_012304.2:g.9597G=
NG_053116.1:g.13277C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.931G= MANE Select	ENSP00000309953.6:p.Asp311=
ENST00000307998.10:c.931G=	ENSP00000309953.6:p.Asp311=
ENST00000525392.1:n.92G=
ENST00000526628.5:n.1497G=
ENST00000528176.5:c.931G=	ENSP00000434151.1:p.Asp311=
ENST00000528409.1:n.175G=
ENST00000530806.5:c.-68G=	ENSP00000436526.1:n.-68G=
ENST00000531005.5:n.1925G=
ENST00000531645.5:c.79G=	ENSP00000436521.1:p.Asp27=
ENST00000531972.5:c.931G=	ENSP00000435295.1:p.Asp311=
ENST00000532084.5:n.357G=
NM_016938.4:c.931G=	NP_058634.4:p.Asp311=
NR_037718.1:n.1190G=
NM_016938.5:c.931G= MANE Select	NP_058634.4:p.Asp311=
NR_037718.2:n.1056G=