Canonical Allele Identifier: CA2574880495
Gene: EFEMP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65871464del , CM000673.2:g.65871464del GRCh38
NC_000011.9:g.65638935del , CM000673.1:g.65638935del GRCh37
NC_000011.8:g.65395511del NCBI36
NG_012304.2:g.6474del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.161-98del MANE Select ENSP00000309953.6:n.161-98del
ENST00000307998.10:c.161-98del ENSP00000309953.6:n.161-98del
ENST00000526624.5:c.161-98del ENSP00000435419.1:n.161-98del
ENST00000527378.1:c.161-98del ENSP00000435963.1:n.161-98del
ENST00000528176.5:c.161-98del ENSP00000434151.1:n.161-98del
ENST00000529870.1:n.766del
ENST00000530850.1:c.150-98del ENSP00000437238.1:n.150-98del
ENST00000531005.5:n.559del
ENST00000531972.5:c.161-98del ENSP00000435295.1:n.161-98del
ENST00000533347.5:c.161-52del ENSP00000435823.1:n.161-52del
NM_016938.4:c.161-98del NP_058634.4:n.161-98del
NR_037718.1:n.420-98del
NM_016938.5:c.161-98del MANE Select NP_058634.4:n.161-98del
NR_037718.2:n.286-98del