Canonical Allele Identifier: CA394303702
Gene: GFER HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985876A>T , CM000678.2:g.1985876A>T GRCh38
NC_000016.9:g.2035877A>T , CM000678.1:g.2035877A>T GRCh37
NC_000016.8:g.1975878A>T NCBI36
NG_016288.1:g.6728A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.241A>T ENSP00000455885.1:p.Asn81Tyr
ENST00000248114.7:c.466A>T MANE Select ENSP00000248114.6:p.Asn156Tyr
ENST00000248114.6:c.466A>T ENSP00000248114.6:p.Asn156Tyr
ENST00000565658.1:n.623A>T
ENST00000567719.1:c.241A>T ENSP00000455885.1:p.Asn81Tyr
ENST00000569451.1:c.269A>T ENSP00000456432.1:p.Glu90Val
NM_005262.2:c.466A>T NP_005253.3:p.Asn156Tyr
NM_005262.3:c.466A>T MANE Select NP_005253.3:p.Asn156Tyr