Canonical Allele Identifier: CA2201967660
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985843_1985844delinsCT , CM000678.2:g.1985843_1985844delinsCT GRCh38
NC_000016.9:g.2035844_2035845delinsCT , CM000678.1:g.2035844_2035845delinsCT GRCh37
NC_000016.8:g.1975845_1975846delinsCT NCBI36
NG_016288.1:g.6695_6696delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.231-23_231-22delinsCT ENSP00000455885.1:n.231-23_231-22delinsCT
ENST00000248114.7:c.456-23_456-22delinsCT MANE Select ENSP00000248114.6:n.456-23_456-22delinsCT
ENST00000248114.6:c.456-23_456-22delinsCT ENSP00000248114.6:n.456-23_456-22delinsCT
ENST00000565658.1:n.613-23_613-22delinsCT
ENST00000567719.1:c.231-23_231-22delinsCT ENSP00000455885.1:n.231-23_231-22delinsCT
ENST00000569451.1:c.259-23_259-22delinsCT ENSP00000456432.1:n.259-23_259-22delinsCT
NM_005262.2:c.456-23_456-22delinsCT NP_005253.3:n.456-23_456-22delinsCT
NM_005262.3:c.456-23_456-22delinsCT MANE Select NP_005253.3:n.456-23_456-22delinsCT