Canonical Allele Identifier: CA1979445104
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65868700C= , CM000673.2:g.65868700C= GRCh38
NC_000011.9:g.65636171C= , CM000673.1:g.65636171C= GRCh37
NC_000011.8:g.65392747C= NCBI36
NG_012304.2:g.9235G=
NG_053116.1:g.13639C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.728-71G= MANE Select ENSP00000309953.6:n.728-71G=
ENST00000307998.10:c.728-71G= ENSP00000309953.6:n.728-71G=
ENST00000526628.5:n.1223G=
ENST00000527969.1:n.1342G=
ENST00000528176.5:c.728-71G= ENSP00000434151.1:n.728-71G=
ENST00000531005.5:n.1722-71G=
ENST00000531972.5:c.728-71G= ENSP00000435295.1:n.728-71G=
ENST00000532084.5:n.154-71G=
NM_016938.4:c.728-71G= NP_058634.4:n.728-71G=
NR_037718.1:n.987-71G=
NM_016938.5:c.728-71G= MANE Select NP_058634.4:n.728-71G=
NR_037718.2:n.853-71G=