Canonical Allele Identifier: CA2201967707
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985892G= , CM000678.2:g.1985892G= GRCh38
NC_000016.9:g.2035893G= , CM000678.1:g.2035893G= GRCh37
NC_000016.8:g.1975894G= NCBI36
NG_016288.1:g.6744G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.257G= ENSP00000455885.1:p.Arg86=
ENST00000248114.7:c.482G= MANE Select ENSP00000248114.6:p.Arg161=
ENST00000248114.6:c.482G= ENSP00000248114.6:p.Arg161=
ENST00000565658.1:n.639G=
ENST00000567719.1:c.257G= ENSP00000455885.1:p.Arg86=
ENST00000569451.1:c.285G= ENSP00000456432.1:p.Pro95=
NM_005262.2:c.482G= NP_005253.3:p.Arg161=
NM_005262.3:c.482G= MANE Select NP_005253.3:p.Arg161=