Canonical Allele Identifier: CA2201967753
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985933A= , CM000678.2:g.1985933A= GRCh38
NC_000016.9:g.2035934A= , CM000678.1:g.2035934A= GRCh37
NC_000016.8:g.1975935A= NCBI36
NG_016288.1:g.6785A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.298A= ENSP00000455885.1:p.Asn100=
ENST00000248114.7:c.523A= MANE Select ENSP00000248114.6:p.Asn175=
ENST00000248114.6:c.523A= ENSP00000248114.6:p.Asn175=
ENST00000565658.1:n.680A=
ENST00000567719.1:c.298A= ENSP00000455885.1:p.Asn100=
ENST00000569451.1:c.326A= ENSP00000456432.1:p.Gln109=
NM_005262.2:c.523A= NP_005253.3:p.Asn175=
NM_005262.3:c.523A= MANE Select NP_005253.3:p.Asn175=