Canonical Allele Identifier: CA2574880398
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868710del , CM000673.2:g.65868710del GRCh38
NC_000011.9:g.65636181del , CM000673.1:g.65636181del GRCh37
NC_000011.8:g.65392757del NCBI36
NG_012304.2:g.9227del
NG_053116.1:g.13649del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.728-79del MANE Select ENSP00000309953.6:n.728-79del
ENST00000307998.10:c.728-79del ENSP00000309953.6:n.728-79del
ENST00000526628.5:n.1215del
ENST00000527969.1:n.1334del
ENST00000528176.5:c.728-79del ENSP00000434151.1:n.728-79del
ENST00000531005.5:n.1722-79del
ENST00000531972.5:c.728-79del ENSP00000435295.1:n.728-79del
ENST00000532084.5:n.154-79del
NM_016938.4:c.728-79del NP_058634.4:n.728-79del
NR_037718.1:n.987-79del
NM_016938.5:c.728-79del MANE Select NP_058634.4:n.728-79del
NR_037718.2:n.853-79del