Canonical Allele Identifier: CA2201967726

Gene: GFER

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1985910C= , CM000678.2:g.1985910C=	GRCh38
NC_000016.9:g.2035911C= , CM000678.1:g.2035911C=	GRCh37
NC_000016.8:g.1975912C=	NCBI36
NG_016288.1:g.6762C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000567719.2:c.275C=	ENSP00000455885.1:p.Thr92=
ENST00000248114.7:c.500C= MANE Select	ENSP00000248114.6:p.Thr167=
ENST00000248114.6:c.500C=	ENSP00000248114.6:p.Thr167=
ENST00000565658.1:n.657C=
ENST00000567719.1:c.275C=	ENSP00000455885.1:p.Thr92=
ENST00000569451.1:c.303C=	ENSP00000456432.1:p.His101=
NM_005262.2:c.500C=	NP_005253.3:p.Thr167=
NM_005262.3:c.500C= MANE Select	NP_005253.3:p.Thr167=