Canonical Allele Identifier: CA372468488

Gene: FAM83H

Linked Data

• dbSNP Id: rs1818387279
• MyVariant Identifiers: chr8:g.144810516C>T (hg19) ; chr8:g.143728346C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728346C>T , CM000670.2:g.143728346C>T	GRCh38
NC_000008.10:g.144810516C>T , CM000670.1:g.144810516C>T	GRCh37
NC_000008.9:g.144882504C>T	NCBI36
NG_016652.1:g.10399G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.1115G>A MANE Select	ENSP00000373565.3:p.Gly372Glu
ENST00000650760.1:c.1718G>A	ENSP00000499217.1:p.Gly573Glu
ENST00000388913.3:c.1115G>A	ENSP00000373565.3:p.Gly372Glu
ENST00000395103.2:c.295G>A
NM_198488.3:c.1115G>A	NP_940890.3:p.Gly372Glu
XM_005250887.2:c.1172G>A	XP_005250944.1:p.Gly391Glu
XM_005250888.2:c.1133G>A	XP_005250945.1:p.Gly378Glu
XM_005250889.2:c.1115G>A	XP_005250946.1:p.Gly372Glu
XM_011516980.1:c.1436G>A	XP_011515282.1:p.Gly479Glu
XM_011516981.1:c.1283G>A	XP_011515283.1:p.Gly428Glu
XM_005250887.3:c.1172G>A	XP_005250944.1:p.Gly391Glu
XM_005250888.3:c.1133G>A	XP_005250945.1:p.Gly378Glu
XM_005250889.3:c.1115G>A	XP_005250946.1:p.Gly372Glu
XM_011516980.2:c.1718G>A	XP_011515282.2:p.Gly573Glu
XM_011516981.2:c.1283G>A	XP_011515283.1:p.Gly428Glu
XM_024447131.1:c.1115G>A	XP_024302899.1:p.Gly372Glu
NM_198488.4:c.1115G>A	NP_940890.3:p.Gly372Glu
NM_198488.5:c.1115G>A MANE Select	NP_940890.4:p.Gly372Glu