Canonical Allele Identifier: CA2614413027

Gene: EFEMP2

Linked Data

• gnomAD v4: 11-65871473-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65871473C>T , CM000673.2:g.65871473C>T	GRCh38
NC_000011.9:g.65638944C>T , CM000673.1:g.65638944C>T	GRCh37
NC_000011.8:g.65395520C>T	NCBI36
NG_012304.2:g.6462G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307998.11:c.161-110G>A MANE Select	ENSP00000309953.6:n.161-110G>A
ENST00000307998.10:c.161-110G>A	ENSP00000309953.6:n.161-110G>A
ENST00000526624.5:c.161-110G>A	ENSP00000435419.1:n.161-110G>A
ENST00000527378.1:c.161-110G>A	ENSP00000435963.1:n.161-110G>A
ENST00000528176.5:c.161-110G>A	ENSP00000434151.1:n.161-110G>A
ENST00000529870.1:n.754G>A
ENST00000530850.1:c.150-110G>A	ENSP00000437238.1:n.150-110G>A
ENST00000531005.5:n.547G>A
ENST00000531972.5:c.161-110G>A	ENSP00000435295.1:n.161-110G>A
ENST00000533347.5:c.161-64G>A	ENSP00000435823.1:n.161-64G>A
NM_016938.4:c.161-110G>A	NP_058634.4:n.161-110G>A
NR_037718.1:n.420-110G>A
NM_016938.5:c.161-110G>A MANE Select	NP_058634.4:n.161-110G>A
NR_037718.2:n.286-110G>A