Canonical Allele Identifier: CA381310783
Gene: EFEMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65871973G>A , CM000673.2:g.65871973G>A GRCh38
NC_000011.9:g.65639444G>A , CM000673.1:g.65639444G>A GRCh37
NC_000011.8:g.65396020G>A NCBI36
NG_012304.2:g.5962C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307998.11:c.157C>T MANE Select ENSP00000309953.6:p.Arg53Trp
ENST00000307998.10:c.157C>T ENSP00000309953.6:p.Arg53Trp
ENST00000526624.5:c.157C>T ENSP00000435419.1:p.Arg53Trp
ENST00000527378.1:c.157C>T ENSP00000435963.1:p.Arg53Trp
ENST00000528176.5:c.157C>T ENSP00000434151.1:p.Arg53Trp
ENST00000529870.1:n.254C>T
ENST00000530850.1:c.149+233C>T ENSP00000437238.1:n.149+233C>T
ENST00000531005.5:n.47C>T
ENST00000531972.5:c.157C>T ENSP00000435295.1:p.Arg53Trp
ENST00000533347.5:c.157C>T ENSP00000435823.1:p.Arg53Trp
NM_016938.4:c.157C>T NP_058634.4:p.Arg53Trp
NR_037718.1:n.416C>T
NM_016938.5:c.157C>T MANE Select NP_058634.4:p.Arg53Trp
NR_037718.2:n.282C>T