Canonical Allele Identifier: CA381310657

Gene: EFEMP2

Linked Data

• MyVariant Identifiers: chr11:g.65638832C>A (hg19) ; chr11:g.65871361C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65871361C>A , CM000673.2:g.65871361C>A	GRCh38
NC_000011.9:g.65638832C>A , CM000673.1:g.65638832C>A	GRCh37
NC_000011.8:g.65395408C>A	NCBI36
NG_012304.2:g.6574G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000307998.11:c.163G>T MANE Select	ENSP00000309953.6:p.Val55Phe
ENST00000307998.10:c.163G>T	ENSP00000309953.6:p.Val55Phe
ENST00000526624.5:c.163G>T	ENSP00000435419.1:p.Val55Phe
ENST00000527378.1:c.163G>T	ENSP00000435963.1:p.Val55Phe
ENST00000528176.5:c.163G>T	ENSP00000434151.1:p.Val55Phe
ENST00000530850.1:c.152G>T	ENSP00000437238.1:p.Cys51Phe
ENST00000531005.5:n.659G>T
ENST00000531972.5:c.163G>T	ENSP00000435295.1:p.Val55Phe
ENST00000533347.5:c.209G>T	ENSP00000435823.1:p.Cys70Phe
NM_016938.4:c.163G>T	NP_058634.4:p.Val55Phe
NR_037718.1:n.422G>T
NM_016938.5:c.163G>T MANE Select	NP_058634.4:p.Val55Phe
NR_037718.2:n.288G>T