Canonical Allele Identifier: CA2201967792
Gene: GFER HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.1985960C= , CM000678.2:g.1985960C= GRCh38
NC_000016.9:g.2035961C= , CM000678.1:g.2035961C= GRCh37
NC_000016.8:g.1975962C= NCBI36
NG_016288.1:g.6812C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000567719.2:c.325C= ENSP00000455885.1:p.Pro109=
ENST00000248114.7:c.550C= MANE Select ENSP00000248114.6:p.Pro184=
ENST00000248114.6:c.550C= ENSP00000248114.6:p.Pro184=
ENST00000565658.1:n.707C=
ENST00000567719.1:c.325C= ENSP00000455885.1:p.Pro109=
ENST00000569451.1:c.*23C= ENSP00000456432.1:n.*23C=
NM_005262.2:c.550C= NP_005253.3:p.Pro184=
NM_005262.3:c.550C= MANE Select NP_005253.3:p.Pro184=