Canonical Allele Identifier: CA1979444759
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868581_65868583delinsATG , CM000673.2:g.65868581_65868583delinsATG GRCh38
NC_000011.9:g.65636052_65636054delinsATG , CM000673.1:g.65636052_65636054delinsATG GRCh37
NC_000011.8:g.65392628_65392630delinsATG NCBI36
NG_012304.2:g.9352_9354delinsCAT
NG_053116.1:g.13520_13522delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.774_776delinsCAT MANE Select ENSP00000309953.6:p.Cys258=
ENST00000307998.10:c.774_776delinsCAT ENSP00000309953.6:p.Cys258=
ENST00000526628.5:n.1340_1342delinsCAT
ENST00000527969.1:n.1459_1461delinsCAT
ENST00000528176.5:c.774_776delinsCAT ENSP00000434151.1:p.Cys258=
ENST00000531005.5:n.1768_1770delinsCAT
ENST00000531972.5:c.774_776delinsCAT ENSP00000435295.1:p.Cys258=
ENST00000532084.5:n.200_202delinsCAT
NM_016938.4:c.774_776delinsCAT NP_058634.4:p.Cys258=
NR_037718.1:n.1033_1035delinsCAT
NM_016938.5:c.774_776delinsCAT MANE Select NP_058634.4:p.Cys258=
NR_037718.2:n.899_901delinsCAT