Canonical Allele Identifier: CA1979442901

Gene: EFEMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65870560G= , CM000673.2:g.65870560G=	GRCh38
NC_000011.9:g.65638031G= , CM000673.1:g.65638031G=	GRCh37
NC_000011.8:g.65394607G=	NCBI36
NG_012304.2:g.7375C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.466C= MANE Select	ENSP00000309953.6:p.Arg156=
ENST00000307998.10:c.466C=	ENSP00000309953.6:p.Arg156=
ENST00000526624.5:c.466C=	ENSP00000435419.1:p.Arg156=
ENST00000527378.1:c.466C=	ENSP00000435963.1:p.Arg156=
ENST00000527969.1:n.145C=
ENST00000528176.5:c.466C=	ENSP00000434151.1:p.Arg156=
ENST00000530850.1:c.*278C=	ENSP00000437238.1:n.*278C=
ENST00000531005.5:n.1460C=
ENST00000531972.5:c.466C=	ENSP00000435295.1:p.Arg156=
ENST00000533347.5:c.*278C=	ENSP00000435823.1:n.*278C=
NM_016938.4:c.466C=	NP_058634.4:p.Arg156=
NR_037718.1:n.725C=
NM_016938.5:c.466C= MANE Select	NP_058634.4:p.Arg156=
NR_037718.2:n.591C=