Canonical Allele Identifier: CA372469190

Gene: FAM83H

Linked Data

• MyVariant Identifiers: chr8:g.144810733C>T (hg19) ; chr8:g.143728563C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728563C>T , CM000670.2:g.143728563C>T	GRCh38
NC_000008.10:g.144810733C>T , CM000670.1:g.144810733C>T	GRCh37
NC_000008.9:g.144882721C>T	NCBI36
NG_016652.1:g.10182G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.898G>A MANE Select	ENSP00000373565.3:p.Ala300Thr
ENST00000650760.1:c.1501G>A	ENSP00000499217.1:p.Ala501Thr
ENST00000388913.3:c.898G>A	ENSP00000373565.3:p.Ala300Thr
ENST00000395103.2:c.78G>A
NM_198488.3:c.898G>A	NP_940890.3:p.Ala300Thr
XM_005250887.2:c.955G>A	XP_005250944.1:p.Ala319Thr
XM_005250888.2:c.916G>A	XP_005250945.1:p.Ala306Thr
XM_005250889.2:c.898G>A	XP_005250946.1:p.Ala300Thr
XM_011516980.1:c.1219G>A	XP_011515282.1:p.Ala407Thr
XM_011516981.1:c.1066G>A	XP_011515283.1:p.Ala356Thr
XM_005250887.3:c.955G>A	XP_005250944.1:p.Ala319Thr
XM_005250888.3:c.916G>A	XP_005250945.1:p.Ala306Thr
XM_005250889.3:c.898G>A	XP_005250946.1:p.Ala300Thr
XM_011516980.2:c.1501G>A	XP_011515282.2:p.Ala501Thr
XM_011516981.2:c.1066G>A	XP_011515283.1:p.Ala356Thr
XM_024447131.1:c.898G>A	XP_024302899.1:p.Ala300Thr
NM_198488.4:c.898G>A	NP_940890.3:p.Ala300Thr
NM_198488.5:c.898G>A MANE Select	NP_940890.4:p.Ala300Thr