Canonical Allele Identifier: CA372469049

Gene: FAM83H

Linked Data

• MyVariant Identifiers: chr8:g.144810699A>T (hg19) ; chr8:g.143728529A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728529A>T , CM000670.2:g.143728529A>T	GRCh38
NC_000008.10:g.144810699A>T , CM000670.1:g.144810699A>T	GRCh37
NC_000008.9:g.144882687A>T	NCBI36
NG_016652.1:g.10216T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.932T>A MANE Select	ENSP00000373565.3:p.Val311Asp
ENST00000650760.1:c.1535T>A	ENSP00000499217.1:p.Val512Asp
ENST00000388913.3:c.932T>A	ENSP00000373565.3:p.Val311Asp
ENST00000395103.2:c.112T>A
NM_198488.3:c.932T>A	NP_940890.3:p.Val311Asp
XM_005250887.2:c.989T>A	XP_005250944.1:p.Val330Asp
XM_005250888.2:c.950T>A	XP_005250945.1:p.Val317Asp
XM_005250889.2:c.932T>A	XP_005250946.1:p.Val311Asp
XM_011516980.1:c.1253T>A	XP_011515282.1:p.Val418Asp
XM_011516981.1:c.1100T>A	XP_011515283.1:p.Val367Asp
XM_005250887.3:c.989T>A	XP_005250944.1:p.Val330Asp
XM_005250888.3:c.950T>A	XP_005250945.1:p.Val317Asp
XM_005250889.3:c.932T>A	XP_005250946.1:p.Val311Asp
XM_011516980.2:c.1535T>A	XP_011515282.2:p.Val512Asp
XM_011516981.2:c.1100T>A	XP_011515283.1:p.Val367Asp
XM_024447131.1:c.932T>A	XP_024302899.1:p.Val311Asp
NM_198488.4:c.932T>A	NP_940890.3:p.Val311Asp
NM_198488.5:c.932T>A MANE Select	NP_940890.4:p.Val311Asp