Canonical Allele Identifier: CA2201967812
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985977A= , CM000678.2:g.1985977A= GRCh38
NC_000016.9:g.2035978A= , CM000678.1:g.2035978A= GRCh37
NC_000016.8:g.1975979A= NCBI36
NG_016288.1:g.6829A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.342A= ENSP00000455885.1:p.Ser114=
ENST00000248114.7:c.567A= MANE Select ENSP00000248114.6:p.Ser189=
ENST00000248114.6:c.567A= ENSP00000248114.6:p.Ser189=
ENST00000565658.1:n.724A=
ENST00000567719.1:c.342A= ENSP00000455885.1:p.Ser114=
ENST00000569451.1:c.*40A= ENSP00000456432.1:n.*40A=
NM_005262.2:c.567A= NP_005253.3:p.Ser189=
NM_005262.3:c.567A= MANE Select NP_005253.3:p.Ser189=