Canonical Allele Identifier: CA1979443871

Gene: EFEMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868335T= , CM000673.2:g.65868335T=	GRCh38
NC_000011.9:g.65635806T= , CM000673.1:g.65635806T=	GRCh37
NC_000011.8:g.65392382T=	NCBI36
NG_012304.2:g.9600A=
NG_053116.1:g.13274T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.934A= MANE Select	ENSP00000309953.6:p.Thr312=
ENST00000307998.10:c.934A=	ENSP00000309953.6:p.Thr312=
ENST00000525392.1:n.95A=
ENST00000526628.5:n.1500A=
ENST00000528176.5:c.934A=	ENSP00000434151.1:p.Thr312=
ENST00000528409.1:n.178A=
ENST00000530806.5:c.-65A=	ENSP00000436526.1:n.-65A=
ENST00000531005.5:n.1928A=
ENST00000531645.5:c.82A=	ENSP00000436521.1:p.Thr28=
ENST00000531972.5:c.934A=	ENSP00000435295.1:p.Thr312=
ENST00000532084.5:n.360A=
NM_016938.4:c.934A=	NP_058634.4:p.Thr312=
NR_037718.1:n.1193A=
NM_016938.5:c.934A= MANE Select	NP_058634.4:p.Thr312=
NR_037718.2:n.1059A=