Canonical Allele Identifier: CA2201967653
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985835C= , CM000678.2:g.1985835C= GRCh38
NC_000016.9:g.2035836C= , CM000678.1:g.2035836C= GRCh37
NC_000016.8:g.1975837C= NCBI36
NG_016288.1:g.6687C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.231-31C= ENSP00000455885.1:n.231-31C=
ENST00000248114.7:c.456-31C= MANE Select ENSP00000248114.6:n.456-31C=
ENST00000248114.6:c.456-31C= ENSP00000248114.6:n.456-31C=
ENST00000565658.1:n.613-31C=
ENST00000567719.1:c.231-31C= ENSP00000455885.1:n.231-31C=
ENST00000569451.1:c.259-31C= ENSP00000456432.1:n.259-31C=
NM_005262.2:c.456-31C= NP_005253.3:n.456-31C=
NM_005262.3:c.456-31C= MANE Select NP_005253.3:n.456-31C=