Canonical Allele Identifier: CA1979442892

Gene: EFEMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65870559C= , CM000673.2:g.65870559C=	GRCh38
NC_000011.9:g.65638030C= , CM000673.1:g.65638030C=	GRCh37
NC_000011.8:g.65394606C=	NCBI36
NG_012304.2:g.7376G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.467G= MANE Select	ENSP00000309953.6:p.Arg156=
ENST00000307998.10:c.467G=	ENSP00000309953.6:p.Arg156=
ENST00000526624.5:c.467G=	ENSP00000435419.1:p.Arg156=
ENST00000527378.1:c.467G=	ENSP00000435963.1:p.Arg156=
ENST00000527969.1:n.146G=
ENST00000528176.5:c.467G=	ENSP00000434151.1:p.Arg156=
ENST00000530850.1:c.*279G=	ENSP00000437238.1:n.*279G=
ENST00000531005.5:n.1461G=
ENST00000531972.5:c.467G=	ENSP00000435295.1:p.Arg156=
ENST00000533347.5:c.*279G=	ENSP00000435823.1:n.*279G=
NM_016938.4:c.467G=	NP_058634.4:p.Arg156=
NR_037718.1:n.726G=
NM_016938.5:c.467G= MANE Select	NP_058634.4:p.Arg156=
NR_037718.2:n.592G=