Canonical Allele Identifier: CA2201967625
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985812A= , CM000678.2:g.1985812A= GRCh38
NC_000016.9:g.2035813A= , CM000678.1:g.2035813A= GRCh37
NC_000016.8:g.1975814A= NCBI36
NG_016288.1:g.6664A=

Transcript Alleles

HGVS Amino-acid change
ENST00000567719.2:c.231-54A= ENSP00000455885.1:n.231-54A=
ENST00000248114.7:c.456-54A= MANE Select ENSP00000248114.6:n.456-54A=
ENST00000248114.6:c.456-54A= ENSP00000248114.6:n.456-54A=
ENST00000565658.1:n.613-54A=
ENST00000567719.1:c.231-54A= ENSP00000455885.1:n.231-54A=
ENST00000569451.1:c.259-54A= ENSP00000456432.1:n.259-54A=
NM_005262.2:c.456-54A= NP_005253.3:n.456-54A=
NM_005262.3:c.456-54A= MANE Select NP_005253.3:n.456-54A=