Canonical Allele Identifier: CA2201967668
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985850T= , CM000678.2:g.1985850T= GRCh38
NC_000016.9:g.2035851T= , CM000678.1:g.2035851T= GRCh37
NC_000016.8:g.1975852T= NCBI36
NG_016288.1:g.6702T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.231-16T= ENSP00000455885.1:n.231-16T=
ENST00000248114.7:c.456-16T= MANE Select ENSP00000248114.6:n.456-16T=
ENST00000248114.6:c.456-16T= ENSP00000248114.6:n.456-16T=
ENST00000565658.1:n.613-16T=
ENST00000567719.1:c.231-16T= ENSP00000455885.1:n.231-16T=
ENST00000569451.1:c.259-16T= ENSP00000456432.1:n.259-16T=
NM_005262.2:c.456-16T= NP_005253.3:n.456-16T=
NM_005262.3:c.456-16T= MANE Select NP_005253.3:n.456-16T=