Canonical Allele Identifier: CA463520121

Gene: FAM83H

Linked Data

• gnomAD v4: 8-143728645-C-T
• MyVariant Identifiers: chr8:g.144810815C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728645C>T , CM000670.2:g.143728645C>T	GRCh38
NC_000008.10:g.144810815C>T , CM000670.1:g.144810815C>T	GRCh37
NC_000008.9:g.144882803C>T	NCBI36
NG_016652.1:g.10100G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.816G>A MANE Select	ENSP00000373565.3:p.Glu272=
ENST00000650760.1:c.1419G>A	ENSP00000499217.1:p.Glu473=
ENST00000388913.3:c.816G>A	ENSP00000373565.3:p.Glu272=
NM_198488.3:c.816G>A	NP_940890.3:p.Glu272=
XM_005250887.2:c.873G>A	XP_005250944.1:p.Glu291=
XM_005250888.2:c.834G>A	XP_005250945.1:p.Glu278=
XM_005250889.2:c.816G>A	XP_005250946.1:p.Glu272=
XM_011516980.1:c.1137G>A	XP_011515282.1:p.Glu379=
XM_011516981.1:c.984G>A	XP_011515283.1:p.Glu328=
XM_005250887.3:c.873G>A	XP_005250944.1:p.Glu291=
XM_005250888.3:c.834G>A	XP_005250945.1:p.Glu278=
XM_005250889.3:c.816G>A	XP_005250946.1:p.Glu272=
XM_011516980.2:c.1419G>A	XP_011515282.2:p.Glu473=
XM_011516981.2:c.984G>A	XP_011515283.1:p.Glu328=
XM_024447131.1:c.816G>A	XP_024302899.1:p.Glu272=
NM_198488.4:c.816G>A	NP_940890.3:p.Glu272=
NM_198488.5:c.816G>A MANE Select	NP_940890.4:p.Glu272=