Canonical Allele Identifier: CA2201967787
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985955G= , CM000678.2:g.1985955G= GRCh38
NC_000016.9:g.2035956G= , CM000678.1:g.2035956G= GRCh37
NC_000016.8:g.1975957G= NCBI36
NG_016288.1:g.6807G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.320G= ENSP00000455885.1:p.Gly107=
ENST00000248114.7:c.545G= MANE Select ENSP00000248114.6:p.Gly182=
ENST00000248114.6:c.545G= ENSP00000248114.6:p.Gly182=
ENST00000565658.1:n.702G=
ENST00000567719.1:c.320G= ENSP00000455885.1:p.Gly107=
ENST00000569451.1:c.*18G= ENSP00000456432.1:n.*18G=
NM_005262.2:c.545G= NP_005253.3:p.Gly182=
NM_005262.3:c.545G= MANE Select NP_005253.3:p.Gly182=