Canonical Allele Identifier: CA2631092383
Gene: GFER HGNC NCBI

Linked Data

gnomAD v4: 16-1985816-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985817del , CM000678.2:g.1985817del GRCh38
NC_000016.9:g.2035818del , CM000678.1:g.2035818del GRCh37
NC_000016.8:g.1975819del NCBI36
NG_016288.1:g.6669del

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.231-49del ENSP00000455885.1:n.231-49del
ENST00000248114.7:c.456-49del MANE Select ENSP00000248114.6:n.456-49del
ENST00000248114.6:c.456-49del ENSP00000248114.6:n.456-49del
ENST00000565658.1:n.613-49del
ENST00000567719.1:c.231-49del ENSP00000455885.1:n.231-49del
ENST00000569451.1:c.259-49del ENSP00000456432.1:n.259-49del
NM_005262.2:c.456-49del NP_005253.3:n.456-49del
NM_005262.3:c.456-49del MANE Select NP_005253.3:n.456-49del
Search 100 bp 5'
Search 100 bp 3'