Canonical Allele Identifier: CA2201967659
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985840A= , CM000678.2:g.1985840A= GRCh38
NC_000016.9:g.2035841A= , CM000678.1:g.2035841A= GRCh37
NC_000016.8:g.1975842A= NCBI36
NG_016288.1:g.6692A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.231-26A= ENSP00000455885.1:n.231-26A=
ENST00000248114.7:c.456-26A= MANE Select ENSP00000248114.6:n.456-26A=
ENST00000248114.6:c.456-26A= ENSP00000248114.6:n.456-26A=
ENST00000565658.1:n.613-26A=
ENST00000567719.1:c.231-26A= ENSP00000455885.1:n.231-26A=
ENST00000569451.1:c.259-26A= ENSP00000456432.1:n.259-26A=
NM_005262.2:c.456-26A= NP_005253.3:n.456-26A=
NM_005262.3:c.456-26A= MANE Select NP_005253.3:n.456-26A=