Canonical Allele Identifier: CA2201967709
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985894A= , CM000678.2:g.1985894A= GRCh38
NC_000016.9:g.2035895A= , CM000678.1:g.2035895A= GRCh37
NC_000016.8:g.1975896A= NCBI36
NG_016288.1:g.6746A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.259A= ENSP00000455885.1:p.Thr87=
ENST00000248114.7:c.484A= MANE Select ENSP00000248114.6:p.Thr162=
ENST00000248114.6:c.484A= ENSP00000248114.6:p.Thr162=
ENST00000565658.1:n.641A=
ENST00000567719.1:c.259A= ENSP00000455885.1:p.Thr87=
ENST00000569451.1:c.287A= ENSP00000456432.1:p.His96=
NM_005262.2:c.484A= NP_005253.3:p.Thr162=
NM_005262.3:c.484A= MANE Select NP_005253.3:p.Thr162=