Canonical Allele Identifier: CA1979443561

Gene: EFEMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868246C= , CM000673.2:g.65868246C=	GRCh38
NC_000011.9:g.65635717C= , CM000673.1:g.65635717C=	GRCh37
NC_000011.8:g.65392293C=	NCBI36
NG_012304.2:g.9689G=
NG_053116.1:g.13185C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.974+49G= MANE Select	ENSP00000309953.6:n.974+49G=
ENST00000307998.10:c.974+49G=	ENSP00000309953.6:n.974+49G=
ENST00000525392.1:n.135+49G=
ENST00000526628.5:n.1540+49G=
ENST00000528176.5:c.974+49G=	ENSP00000434151.1:n.974+49G=
ENST00000528409.1:n.207+60G=
ENST00000530806.5:c.-25+49G=	ENSP00000436526.1:n.-25+49G=
ENST00000531005.5:n.1968+49G=
ENST00000531645.5:c.122+49G=	ENSP00000436521.1:n.122+49G=
ENST00000531972.5:c.974+49G=	ENSP00000435295.1:n.974+49G=
ENST00000532084.5:n.400+49G=
NM_016938.4:c.974+49G=	NP_058634.4:n.974+49G=
NR_037718.1:n.1233+49G=
NM_016938.5:c.974+49G= MANE Select	NP_058634.4:n.974+49G=
NR_037718.2:n.1099+49G=