Canonical Allele Identifier: CA1979443555

Gene: EFEMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868244G= , CM000673.2:g.65868244G=	GRCh38
NC_000011.9:g.65635715G= , CM000673.1:g.65635715G=	GRCh37
NC_000011.8:g.65392291G=	NCBI36
NG_012304.2:g.9691C=
NG_053116.1:g.13183G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.974+51C= MANE Select	ENSP00000309953.6:n.974+51C=
ENST00000307998.10:c.974+51C=	ENSP00000309953.6:n.974+51C=
ENST00000525392.1:n.135+51C=
ENST00000526628.5:n.1540+51C=
ENST00000528176.5:c.974+51C=	ENSP00000434151.1:n.974+51C=
ENST00000528409.1:n.207+62C=
ENST00000530806.5:c.-25+51C=	ENSP00000436526.1:n.-25+51C=
ENST00000531005.5:n.1968+51C=
ENST00000531645.5:c.122+51C=	ENSP00000436521.1:n.122+51C=
ENST00000531972.5:c.974+51C=	ENSP00000435295.1:n.974+51C=
ENST00000532084.5:n.400+51C=
NM_016938.4:c.974+51C=	NP_058634.4:n.974+51C=
NR_037718.1:n.1233+51C=
NM_016938.5:c.974+51C= MANE Select	NP_058634.4:n.974+51C=
NR_037718.2:n.1099+51C=