Canonical Allele Identifier: CA475296360
Community Standard Title: NM_016938.5(EFEMP2):c.321C>T (p.Asn107=)
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65871203G>A , CM000673.2:g.65871203G>A GRCh38
NC_000011.9:g.65638674G>A , CM000673.1:g.65638674G>A GRCh37
NC_000011.8:g.65395250G>A NCBI36
NG_012304.2:g.6732C>T

Transcript Alleles

HGVS Amino-acid Change
NM_016938.5:c.321C>T MANE Select NP_058634.4:p.Asn107=
ENST00000307998.11:c.321C>T MANE Select ENSP00000309953.6:p.Asn107=
NM_016938.4:c.321C>T NP_058634.4:p.Asn107=
NR_037718.1:n.580C>T
NR_037718.2:n.446C>T
ENST00000307998.10:c.321C>T ENSP00000309953.6:p.Asn107=
ENST00000526624.5:c.321C>T ENSP00000435419.1:p.Asn107=
ENST00000527378.1:c.321C>T ENSP00000435963.1:p.Asn107=
ENST00000528176.5:c.321C>T ENSP00000434151.1:p.Asn107=
ENST00000530850.1:c.*133C>T ENSP00000437238.1:n.*133C>T
ENST00000531005.5:n.817C>T
ENST00000531972.5:c.321C>T ENSP00000435295.1:p.Asn107=
ENST00000533347.5:c.*133C>T ENSP00000435823.1:n.*133C>T