Canonical Allele Identifier: CA620704190
Gene: GFER HGNC NCBI

Linked Data

dbSNP Id: rs1382730751

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985846del , CM000678.2:g.1985846del GRCh38
NC_000016.9:g.2035847del , CM000678.1:g.2035847del GRCh37
NC_000016.8:g.1975848del NCBI36
NG_016288.1:g.6698del

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.231-20del ENSP00000455885.1:n.231-20del
ENST00000248114.7:c.456-20del MANE Select ENSP00000248114.6:n.456-20del
ENST00000248114.6:c.456-20del ENSP00000248114.6:n.456-20del
ENST00000565658.1:n.613-20del
ENST00000567719.1:c.231-20del ENSP00000455885.1:n.231-20del
ENST00000569451.1:c.259-20del ENSP00000456432.1:n.259-20del
NM_005262.2:c.456-20del NP_005253.3:n.456-20del
NM_005262.3:c.456-20del MANE Select NP_005253.3:n.456-20del