Canonical Allele Identifier: CA475316727

Gene: EFEMP2

Linked Data

• MyVariant Identifiers: chr11:g.65635994T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868523T>A , CM000673.2:g.65868523T>A	GRCh38
NC_000011.9:g.65635994T>A , CM000673.1:g.65635994T>A	GRCh37
NC_000011.8:g.65392570T>A	NCBI36
NG_012304.2:g.9412A>T
NG_053116.1:g.13462T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.834A>T MANE Select	ENSP00000309953.6:p.Thr278=
ENST00000307998.10:c.834A>T	ENSP00000309953.6:p.Thr278=
ENST00000526628.5:n.1400A>T
ENST00000527969.1:n.1519A>T
ENST00000528176.5:c.834A>T	ENSP00000434151.1:p.Thr278=
ENST00000530806.5:c.-165A>T	ENSP00000436526.1:n.-165A>T
ENST00000531005.5:n.1828A>T
ENST00000531972.5:c.834A>T	ENSP00000435295.1:p.Thr278=
ENST00000532084.5:n.260A>T
NM_016938.4:c.834A>T	NP_058634.4:p.Thr278=
NR_037718.1:n.1093A>T
NM_016938.5:c.834A>T MANE Select	NP_058634.4:p.Thr278=
NR_037718.2:n.959A>T