Canonical Allele Identifier: CA394303638

Gene: GFER

Linked Data

• gnomAD v4: 16-1985866-G-T
• MyVariant Identifiers: chr16:g.2035867G>T (hg19) ; chr16:g.1985866G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.1985866G>T , CM000678.2:g.1985866G>T	GRCh38
NC_000016.9:g.2035867G>T , CM000678.1:g.2035867G>T	GRCh37
NC_000016.8:g.1975868G>T	NCBI36
NG_016288.1:g.6718G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567719.2:c.231G>T	ENSP00000455885.1:p.Arg77Ser
ENST00000248114.7:c.456G>T MANE Select	ENSP00000248114.6:p.Arg152Ser
ENST00000248114.6:c.456G>T	ENSP00000248114.6:p.Arg152Ser
ENST00000565658.1:n.613G>T
ENST00000567719.1:c.231G>T	ENSP00000455885.1:p.Arg77Ser
ENST00000569451.1:c.259G>T	ENSP00000456432.1:p.Ala87Ser
NM_005262.2:c.456G>T	NP_005253.3:p.Arg152Ser
NM_005262.3:c.456G>T MANE Select	NP_005253.3:p.Arg152Ser