Canonical Allele Identifier: CA2201967914
Gene: GFER HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1986042A= , CM000678.2:g.1986042A= GRCh38
NC_000016.9:g.2036043A= , CM000678.1:g.2036043A= GRCh37
NC_000016.8:g.1976044A= NCBI36
NG_016288.1:g.6894A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.*14A= ENSP00000455885.1:n.*14A=
ENST00000248114.7:c.*14A= MANE Select ENSP00000248114.6:n.*14A=
ENST00000248114.6:c.*14A= ENSP00000248114.6:n.*14A=
ENST00000565658.1:n.789A=
ENST00000567719.1:c.*14A= ENSP00000455885.1:n.*14A=
ENST00000569451.1:c.*105A= ENSP00000456432.1:n.*105A=
NM_005262.2:c.*14A= NP_005253.3:n.*14A=
NM_005262.3:c.*14A= MANE Select NP_005253.3:n.*14A=
Search 100 bp 5'
Search 100 bp 3'