Canonical Allele Identifier: CA381356926
Gene: EFEMP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868576C>A , CM000673.2:g.65868576C>A GRCh38
NC_000011.9:g.65636047C>A , CM000673.1:g.65636047C>A GRCh37
NC_000011.8:g.65392623C>A NCBI36
NG_012304.2:g.9359G>T
NG_053116.1:g.13515C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.781G>T MANE Select ENSP00000309953.6:p.Glu261Ter
ENST00000307998.10:c.781G>T ENSP00000309953.6:p.Glu261Ter
ENST00000526628.5:n.1347G>T
ENST00000527969.1:n.1466G>T
ENST00000528176.5:c.781G>T ENSP00000434151.1:p.Glu261Ter
ENST00000531005.5:n.1775G>T
ENST00000531972.5:c.781G>T ENSP00000435295.1:p.Glu261Ter
ENST00000532084.5:n.207G>T
NM_016938.4:c.781G>T NP_058634.4:p.Glu261Ter
NR_037718.1:n.1040G>T
NM_016938.5:c.781G>T MANE Select NP_058634.4:p.Glu261Ter
NR_037718.2:n.906G>T