Canonical Allele Identifier: CA381354480

Gene: EFEMP2

Linked Data

• gnomAD v4: 11-65868519-G-A
• MyVariant Identifiers: chr11:g.65635990G>A (hg19) ; chr11:g.65868519G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65868519G>A , CM000673.2:g.65868519G>A	GRCh38
NC_000011.9:g.65635990G>A , CM000673.1:g.65635990G>A	GRCh37
NC_000011.8:g.65392566G>A	NCBI36
NG_012304.2:g.9416C>T
NG_053116.1:g.13458G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.838C>T MANE Select	ENSP00000309953.6:p.Leu280Phe
ENST00000307998.10:c.838C>T	ENSP00000309953.6:p.Leu280Phe
ENST00000526628.5:n.1404C>T
ENST00000527969.1:n.1523C>T
ENST00000528176.5:c.838C>T	ENSP00000434151.1:p.Leu280Phe
ENST00000530806.5:c.-161C>T	ENSP00000436526.1:n.-161C>T
ENST00000531005.5:n.1832C>T
ENST00000531972.5:c.838C>T	ENSP00000435295.1:p.Leu280Phe
ENST00000532084.5:n.264C>T
NM_016938.4:c.838C>T	NP_058634.4:p.Leu280Phe
NR_037718.1:n.1097C>T
NM_016938.5:c.838C>T MANE Select	NP_058634.4:p.Leu280Phe
NR_037718.2:n.963C>T