Canonical Allele Identifier: CA372469339

Gene: FAM83H

Linked Data

• MyVariant Identifiers: chr8:g.144810777A>G (hg19) ; chr8:g.143728607A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728607A>G , CM000670.2:g.143728607A>G	GRCh38
NC_000008.10:g.144810777A>G , CM000670.1:g.144810777A>G	GRCh37
NC_000008.9:g.144882765A>G	NCBI36
NG_016652.1:g.10138T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.854T>C MANE Select	ENSP00000373565.3:p.Val285Ala
ENST00000650760.1:c.1457T>C	ENSP00000499217.1:p.Val486Ala
ENST00000388913.3:c.854T>C	ENSP00000373565.3:p.Val285Ala
ENST00000395103.2:c.34T>C
NM_198488.3:c.854T>C	NP_940890.3:p.Val285Ala
XM_005250887.2:c.911T>C	XP_005250944.1:p.Val304Ala
XM_005250888.2:c.872T>C	XP_005250945.1:p.Val291Ala
XM_005250889.2:c.854T>C	XP_005250946.1:p.Val285Ala
XM_011516980.1:c.1175T>C	XP_011515282.1:p.Val392Ala
XM_011516981.1:c.1022T>C	XP_011515283.1:p.Val341Ala
XM_005250887.3:c.911T>C	XP_005250944.1:p.Val304Ala
XM_005250888.3:c.872T>C	XP_005250945.1:p.Val291Ala
XM_005250889.3:c.854T>C	XP_005250946.1:p.Val285Ala
XM_011516980.2:c.1457T>C	XP_011515282.2:p.Val486Ala
XM_011516981.2:c.1022T>C	XP_011515283.1:p.Val341Ala
XM_024447131.1:c.854T>C	XP_024302899.1:p.Val285Ala
NM_198488.4:c.854T>C	NP_940890.3:p.Val285Ala
NM_198488.5:c.854T>C MANE Select	NP_940890.4:p.Val285Ala