Canonical Allele Identifier: CA372468982

Gene: FAM83H

Linked Data

• MyVariant Identifiers: chr8:g.144810667A>C (hg19) ; chr8:g.143728497A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728497A>C , CM000670.2:g.143728497A>C	GRCh38
NC_000008.10:g.144810667A>C , CM000670.1:g.144810667A>C	GRCh37
NC_000008.9:g.144882655A>C	NCBI36
NG_016652.1:g.10248T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.964T>G MANE Select	ENSP00000373565.3:p.Phe322Val
ENST00000650760.1:c.1567T>G	ENSP00000499217.1:p.Phe523Val
ENST00000388913.3:c.964T>G	ENSP00000373565.3:p.Phe322Val
ENST00000395103.2:c.144T>G
NM_198488.3:c.964T>G	NP_940890.3:p.Phe322Val
XM_005250887.2:c.1021T>G	XP_005250944.1:p.Phe341Val
XM_005250888.2:c.982T>G	XP_005250945.1:p.Phe328Val
XM_005250889.2:c.964T>G	XP_005250946.1:p.Phe322Val
XM_011516980.1:c.1285T>G	XP_011515282.1:p.Phe429Val
XM_011516981.1:c.1132T>G	XP_011515283.1:p.Phe378Val
XM_005250887.3:c.1021T>G	XP_005250944.1:p.Phe341Val
XM_005250888.3:c.982T>G	XP_005250945.1:p.Phe328Val
XM_005250889.3:c.964T>G	XP_005250946.1:p.Phe322Val
XM_011516980.2:c.1567T>G	XP_011515282.2:p.Phe523Val
XM_011516981.2:c.1132T>G	XP_011515283.1:p.Phe378Val
XM_024447131.1:c.964T>G	XP_024302899.1:p.Phe322Val
NM_198488.4:c.964T>G	NP_940890.3:p.Phe322Val
NM_198488.5:c.964T>G MANE Select	NP_940890.4:p.Phe322Val