Canonical Allele Identifier: CA475316624

Gene: EFEMP2

Linked Data

• MyVariant Identifiers: chr11:g.65635810C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868339C>T , CM000673.2:g.65868339C>T	GRCh38
NC_000011.9:g.65635810C>T , CM000673.1:g.65635810C>T	GRCh37
NC_000011.8:g.65392386C>T	NCBI36
NG_012304.2:g.9596G>A
NG_053116.1:g.13278C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.930G>A MANE Select	ENSP00000309953.6:p.Val310=
ENST00000307998.10:c.930G>A	ENSP00000309953.6:p.Val310=
ENST00000525392.1:n.91G>A
ENST00000526628.5:n.1496G>A
ENST00000528176.5:c.930G>A	ENSP00000434151.1:p.Val310=
ENST00000528409.1:n.174G>A
ENST00000530806.5:c.-69G>A	ENSP00000436526.1:n.-69G>A
ENST00000531005.5:n.1924G>A
ENST00000531645.5:c.78G>A	ENSP00000436521.1:p.Val26=
ENST00000531972.5:c.930G>A	ENSP00000435295.1:p.Val310=
ENST00000532084.5:n.356G>A
NM_016938.4:c.930G>A	NP_058634.4:p.Val310=
NR_037718.1:n.1189G>A
NM_016938.5:c.930G>A MANE Select	NP_058634.4:p.Val310=
NR_037718.2:n.1055G>A