Canonical Allele Identifier: CA2201967756
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985936G= , CM000678.2:g.1985936G= GRCh38
NC_000016.9:g.2035937G= , CM000678.1:g.2035937G= GRCh37
NC_000016.8:g.1975938G= NCBI36
NG_016288.1:g.6788G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.301G= ENSP00000455885.1:p.Glu101=
ENST00000248114.7:c.526G= MANE Select ENSP00000248114.6:p.Glu176=
ENST00000248114.6:c.526G= ENSP00000248114.6:p.Glu176=
ENST00000565658.1:n.683G=
ENST00000567719.1:c.301G= ENSP00000455885.1:p.Glu101=
ENST00000569451.1:c.329G= ENSP00000456432.1:p.Ter110=
NM_005262.2:c.526G= NP_005253.3:p.Glu176=
NM_005262.3:c.526G= MANE Select NP_005253.3:p.Glu176=