Canonical Allele Identifier: CA1979445127

Gene: EFEMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65871374G= , CM000673.2:g.65871374G=	GRCh38
NC_000011.9:g.65638845G= , CM000673.1:g.65638845G=	GRCh37
NC_000011.8:g.65395421G=	NCBI36
NG_012304.2:g.6561C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000307998.11:c.161-11C= MANE Select	ENSP00000309953.6:n.161-11C=
ENST00000307998.10:c.161-11C=	ENSP00000309953.6:n.161-11C=
ENST00000526624.5:c.161-11C=	ENSP00000435419.1:n.161-11C=
ENST00000527378.1:c.161-11C=	ENSP00000435963.1:n.161-11C=
ENST00000528176.5:c.161-11C=	ENSP00000434151.1:n.161-11C=
ENST00000530850.1:c.150-11C=	ENSP00000437238.1:n.150-11C=
ENST00000531005.5:n.646C=
ENST00000531972.5:c.161-11C=	ENSP00000435295.1:n.161-11C=
ENST00000533347.5:c.196C=	ENSP00000435823.1:p.Pro66=
NM_016938.4:c.161-11C=	NP_058634.4:n.161-11C=
NR_037718.1:n.420-11C=
NM_016938.5:c.161-11C= MANE Select	NP_058634.4:n.161-11C=
NR_037718.2:n.286-11C=