Canonical Allele Identifier: CA381352857

Gene: EFEMP2

Linked Data

• MyVariant Identifiers: chr11:g.65635779G>T (hg19) ; chr11:g.65868308G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868308G>T , CM000673.2:g.65868308G>T	GRCh38
NC_000011.9:g.65635779G>T , CM000673.1:g.65635779G>T	GRCh37
NC_000011.8:g.65392355G>T	NCBI36
NG_012304.2:g.9627C>A
NG_053116.1:g.13247G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.961C>A MANE Select	ENSP00000309953.6:p.Gln321Lys
ENST00000307998.10:c.961C>A	ENSP00000309953.6:p.Gln321Lys
ENST00000525392.1:n.122C>A
ENST00000526628.5:n.1527C>A
ENST00000528176.5:c.961C>A	ENSP00000434151.1:p.Gln321Lys
ENST00000528409.1:n.205C>A
ENST00000530806.5:c.-38C>A	ENSP00000436526.1:n.-38C>A
ENST00000531005.5:n.1955C>A
ENST00000531645.5:c.109C>A	ENSP00000436521.1:p.Gln37Lys
ENST00000531972.5:c.961C>A	ENSP00000435295.1:p.Gln321Lys
ENST00000532084.5:n.387C>A
NM_016938.4:c.961C>A	NP_058634.4:p.Gln321Lys
NR_037718.1:n.1220C>A
NM_016938.5:c.961C>A MANE Select	NP_058634.4:p.Gln321Lys
NR_037718.2:n.1086C>A