Canonical Allele Identifier: CA2201967614
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985797A= , CM000678.2:g.1985797A= GRCh38
NC_000016.9:g.2035798A= , CM000678.1:g.2035798A= GRCh37
NC_000016.8:g.1975799A= NCBI36
NG_016288.1:g.6649A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.231-69A= ENSP00000455885.1:n.231-69A=
ENST00000248114.7:c.456-69A= MANE Select ENSP00000248114.6:n.456-69A=
ENST00000248114.6:c.456-69A= ENSP00000248114.6:n.456-69A=
ENST00000565658.1:n.613-69A=
ENST00000567719.1:c.231-69A= ENSP00000455885.1:n.231-69A=
ENST00000569451.1:c.259-69A= ENSP00000456432.1:n.259-69A=
NM_005262.2:c.456-69A= NP_005253.3:n.456-69A=
NM_005262.3:c.456-69A= MANE Select NP_005253.3:n.456-69A=