Canonical Allele Identifier: CA2201967917
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1986043G= , CM000678.2:g.1986043G= GRCh38
NC_000016.9:g.2036044G= , CM000678.1:g.2036044G= GRCh37
NC_000016.8:g.1976045G= NCBI36
NG_016288.1:g.6895G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.*15G= ENSP00000455885.1:n.*15G=
ENST00000248114.7:c.*15G= MANE Select ENSP00000248114.6:n.*15G=
ENST00000248114.6:c.*15G= ENSP00000248114.6:n.*15G=
ENST00000565658.1:n.790G=
ENST00000567719.1:c.*15G= ENSP00000455885.1:n.*15G=
ENST00000569451.1:c.*106G= ENSP00000456432.1:n.*106G=
NM_005262.2:c.*15G= NP_005253.3:n.*15G=
NM_005262.3:c.*15G= MANE Select NP_005253.3:n.*15G=