Canonical Allele Identifier: CA2201967949
Gene: GFER HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1986063C= , CM000678.2:g.1986063C= GRCh38
NC_000016.9:g.2036064C= , CM000678.1:g.2036064C= GRCh37
NC_000016.8:g.1976065C= NCBI36
NG_016288.1:g.6915C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.*35C= ENSP00000455885.1:n.*35C=
ENST00000248114.7:c.*35C= MANE Select ENSP00000248114.6:n.*35C=
ENST00000248114.6:c.*35C= ENSP00000248114.6:n.*35C=
ENST00000565658.1:n.810C=
ENST00000567719.1:c.*35C= ENSP00000455885.1:n.*35C=
ENST00000569451.1:c.*126C= ENSP00000456432.1:n.*126C=
NM_005262.2:c.*35C= NP_005253.3:n.*35C=
NM_005262.3:c.*35C= MANE Select NP_005253.3:n.*35C=
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