Canonical Allele Identifier: CA475316772

Gene: EFEMP2

Linked Data

• MyVariant Identifiers: chr11:g.65636018T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868547T>G , CM000673.2:g.65868547T>G	GRCh38
NC_000011.9:g.65636018T>G , CM000673.1:g.65636018T>G	GRCh37
NC_000011.8:g.65392594T>G	NCBI36
NG_012304.2:g.9388A>C
NG_053116.1:g.13486T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.810A>C MANE Select	ENSP00000309953.6:p.Pro270=
ENST00000307998.10:c.810A>C	ENSP00000309953.6:p.Pro270=
ENST00000526628.5:n.1376A>C
ENST00000527969.1:n.1495A>C
ENST00000528176.5:c.810A>C	ENSP00000434151.1:p.Pro270=
ENST00000531005.5:n.1804A>C
ENST00000531972.5:c.810A>C	ENSP00000435295.1:p.Pro270=
ENST00000532084.5:n.236A>C
NM_016938.4:c.810A>C	NP_058634.4:p.Pro270=
NR_037718.1:n.1069A>C
NM_016938.5:c.810A>C MANE Select	NP_058634.4:p.Pro270=
NR_037718.2:n.935A>C