Canonical Allele Identifier: CA475316737

Gene: EFEMP2

Linked Data

• MyVariant Identifiers: chr11:g.65635997G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868526G>T , CM000673.2:g.65868526G>T	GRCh38
NC_000011.9:g.65635997G>T , CM000673.1:g.65635997G>T	GRCh37
NC_000011.8:g.65392573G>T	NCBI36
NG_012304.2:g.9409C>A
NG_053116.1:g.13465G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.831C>A MANE Select	ENSP00000309953.6:p.Ala277=
ENST00000307998.10:c.831C>A	ENSP00000309953.6:p.Ala277=
ENST00000526628.5:n.1397C>A
ENST00000527969.1:n.1516C>A
ENST00000528176.5:c.831C>A	ENSP00000434151.1:p.Ala277=
ENST00000530806.5:c.-168C>A	ENSP00000436526.1:n.-168C>A
ENST00000531005.5:n.1825C>A
ENST00000531972.5:c.831C>A	ENSP00000435295.1:p.Ala277=
ENST00000532084.5:n.257C>A
NM_016938.4:c.831C>A	NP_058634.4:p.Ala277=
NR_037718.1:n.1090C>A
NM_016938.5:c.831C>A MANE Select	NP_058634.4:p.Ala277=
NR_037718.2:n.956C>A