Canonical Allele Identifier: CA2201967696
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985874G= , CM000678.2:g.1985874G= GRCh38
NC_000016.9:g.2035875G= , CM000678.1:g.2035875G= GRCh37
NC_000016.8:g.1975876G= NCBI36
NG_016288.1:g.6726G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.239G= ENSP00000455885.1:p.Arg80=
ENST00000248114.7:c.464G= MANE Select ENSP00000248114.6:p.Arg155=
ENST00000248114.6:c.464G= ENSP00000248114.6:p.Arg155=
ENST00000565658.1:n.621G=
ENST00000567719.1:c.239G= ENSP00000455885.1:p.Arg80=
ENST00000569451.1:c.267G= ENSP00000456432.1:p.Gln89=
NM_005262.2:c.464G= NP_005253.3:p.Arg155=
NM_005262.3:c.464G= MANE Select NP_005253.3:p.Arg155=