Canonical Allele Identifier: CA1979443999

Gene: EFEMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868364T= , CM000673.2:g.65868364T=	GRCh38
NC_000011.9:g.65635835T= , CM000673.1:g.65635835T=	GRCh37
NC_000011.8:g.65392411T=	NCBI36
NG_012304.2:g.9571A=
NG_053116.1:g.13303T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.905A= MANE Select	ENSP00000309953.6:p.Asn302=
ENST00000307998.10:c.905A=	ENSP00000309953.6:p.Asn302=
ENST00000525392.1:n.66A=
ENST00000526628.5:n.1471A=
ENST00000528176.5:c.905A=	ENSP00000434151.1:p.Asn302=
ENST00000528409.1:n.149A=
ENST00000530806.5:c.-94A=	ENSP00000436526.1:n.-94A=
ENST00000531005.5:n.1899A=
ENST00000531645.5:c.53A=	ENSP00000436521.1:p.Asn18=
ENST00000531972.5:c.905A=	ENSP00000435295.1:p.Asn302=
ENST00000532084.5:n.331A=
NM_016938.4:c.905A=	NP_058634.4:p.Asn302=
NR_037718.1:n.1164A=
NM_016938.5:c.905A= MANE Select	NP_058634.4:p.Asn302=
NR_037718.2:n.1030A=