Canonical Allele Identifier: CA394303938
Gene: GFER HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985904G>A , CM000678.2:g.1985904G>A GRCh38
NC_000016.9:g.2035905G>A , CM000678.1:g.2035905G>A GRCh37
NC_000016.8:g.1975906G>A NCBI36
NG_016288.1:g.6756G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.269G>A ENSP00000455885.1:p.Cys90Tyr
ENST00000248114.7:c.494G>A MANE Select ENSP00000248114.6:p.Cys165Tyr
ENST00000248114.6:c.494G>A ENSP00000248114.6:p.Cys165Tyr
ENST00000565658.1:n.651G>A
ENST00000567719.1:c.269G>A ENSP00000455885.1:p.Cys90Tyr
ENST00000569451.1:c.297G>A ENSP00000456432.1:p.Met99Ile
NM_005262.2:c.494G>A NP_005253.3:p.Cys165Tyr
NM_005262.3:c.494G>A MANE Select NP_005253.3:p.Cys165Tyr