Canonical Allele Identifier: CA1979444470

Gene: EFEMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868484G= , CM000673.2:g.65868484G=	GRCh38
NC_000011.9:g.65635955G= , CM000673.1:g.65635955G=	GRCh37
NC_000011.8:g.65392531G=	NCBI36
NG_012304.2:g.9451C=
NG_053116.1:g.13423G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.847+26C= MANE Select	ENSP00000309953.6:n.847+26C=
ENST00000307998.10:c.847+26C=	ENSP00000309953.6:n.847+26C=
ENST00000526628.5:n.1413+26C=
ENST00000527969.1:n.1558C=
ENST00000528176.5:c.847+26C=	ENSP00000434151.1:n.847+26C=
ENST00000528409.1:n.29C=
ENST00000530806.5:c.-152+26C=	ENSP00000436526.1:n.-152+26C=
ENST00000531005.5:n.1841+26C=
ENST00000531972.5:c.847+26C=	ENSP00000435295.1:n.847+26C=
ENST00000532084.5:n.273+26C=
NM_016938.4:c.847+26C=	NP_058634.4:n.847+26C=
NR_037718.1:n.1106+26C=
NM_016938.5:c.847+26C= MANE Select	NP_058634.4:n.847+26C=
NR_037718.2:n.972+26C=