Canonical Allele Identifier: CA394303631

Gene: GFER

Linked Data

• MyVariant Identifiers: chr16:g.2035866G>A (hg19) ; chr16:g.1985865G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1985865G>A , CM000678.2:g.1985865G>A	GRCh38
NC_000016.9:g.2035866G>A , CM000678.1:g.2035866G>A	GRCh37
NC_000016.8:g.1975867G>A	NCBI36
NG_016288.1:g.6717G>A

Transcript Alleles

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