Canonical Allele Identifier: CA1979445322

Gene: EFEMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65871437C= , CM000673.2:g.65871437C=	GRCh38
NC_000011.9:g.65638908C= , CM000673.1:g.65638908C=	GRCh37
NC_000011.8:g.65395484C=	NCBI36
NG_012304.2:g.6498G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.161-74G= MANE Select	ENSP00000309953.6:n.161-74G=
ENST00000307998.10:c.161-74G=	ENSP00000309953.6:n.161-74G=
ENST00000526624.5:c.161-74G=	ENSP00000435419.1:n.161-74G=
ENST00000527378.1:c.161-74G=	ENSP00000435963.1:n.161-74G=
ENST00000528176.5:c.161-74G=	ENSP00000434151.1:n.161-74G=
ENST00000529870.1:n.790G=
ENST00000530850.1:c.150-74G=	ENSP00000437238.1:n.150-74G=
ENST00000531005.5:n.583G=
ENST00000531972.5:c.161-74G=	ENSP00000435295.1:n.161-74G=
ENST00000533347.5:c.161-28G=	ENSP00000435823.1:n.161-28G=
NM_016938.4:c.161-74G=	NP_058634.4:n.161-74G=
NR_037718.1:n.420-74G=
NM_016938.5:c.161-74G= MANE Select	NP_058634.4:n.161-74G=
NR_037718.2:n.286-74G=