Canonical Allele Identifier: CA475316799

Gene: EFEMP2

Linked Data

• MyVariant Identifiers: chr11:g.65636042T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868571T>A , CM000673.2:g.65868571T>A	GRCh38
NC_000011.9:g.65636042T>A , CM000673.1:g.65636042T>A	GRCh37
NC_000011.8:g.65392618T>A	NCBI36
NG_012304.2:g.9364A>T
NG_053116.1:g.13510T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.786A>T MANE Select	ENSP00000309953.6:p.Pro262=
ENST00000307998.10:c.786A>T	ENSP00000309953.6:p.Pro262=
ENST00000526628.5:n.1352A>T
ENST00000527969.1:n.1471A>T
ENST00000528176.5:c.786A>T	ENSP00000434151.1:p.Pro262=
ENST00000531005.5:n.1780A>T
ENST00000531972.5:c.786A>T	ENSP00000435295.1:p.Pro262=
ENST00000532084.5:n.212A>T
NM_016938.4:c.786A>T	NP_058634.4:p.Pro262=
NR_037718.1:n.1045A>T
NM_016938.5:c.786A>T MANE Select	NP_058634.4:p.Pro262=
NR_037718.2:n.911A>T