Canonical Allele Identifier: CA1979445094
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868688A= , CM000673.2:g.65868688A= GRCh38
NC_000011.9:g.65636159A= , CM000673.1:g.65636159A= GRCh37
NC_000011.8:g.65392735A= NCBI36
NG_012304.2:g.9247T=
NG_053116.1:g.13627A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.728-59T= MANE Select ENSP00000309953.6:n.728-59T=
ENST00000307998.10:c.728-59T= ENSP00000309953.6:n.728-59T=
ENST00000526628.5:n.1235T=
ENST00000527969.1:n.1354T=
ENST00000528176.5:c.728-59T= ENSP00000434151.1:n.728-59T=
ENST00000531005.5:n.1722-59T=
ENST00000531972.5:c.728-59T= ENSP00000435295.1:n.728-59T=
ENST00000532084.5:n.154-59T=
NM_016938.4:c.728-59T= NP_058634.4:n.728-59T=
NR_037718.1:n.987-59T=
NM_016938.5:c.728-59T= MANE Select NP_058634.4:n.728-59T=
NR_037718.2:n.853-59T=