Canonical Allele Identifier: CA1825940798

Gene: FAM83H

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728484G= , CM000670.2:g.143728484G=	GRCh38
NC_000008.10:g.144810654G= , CM000670.1:g.144810654G=	GRCh37
NC_000008.9:g.144882642G=	NCBI36
NG_016652.1:g.10261C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.977C= MANE Select	ENSP00000373565.3:p.Ala326=
ENST00000650760.1:c.1580C=	ENSP00000499217.1:p.Ala527=
ENST00000388913.3:c.977C=	ENSP00000373565.3:p.Ala326=
ENST00000395103.2:c.157C=
NM_198488.3:c.977C=	NP_940890.3:p.Ala326=
XM_005250887.2:c.1034C=	XP_005250944.1:p.Ala345=
XM_005250888.2:c.995C=	XP_005250945.1:p.Ala332=
XM_005250889.2:c.977C=	XP_005250946.1:p.Ala326=
XM_011516980.1:c.1298C=	XP_011515282.1:p.Ala433=
XM_011516981.1:c.1145C=	XP_011515283.1:p.Ala382=
XM_005250887.3:c.1034C=	XP_005250944.1:p.Ala345=
XM_005250888.3:c.995C=	XP_005250945.1:p.Ala332=
XM_005250889.3:c.977C=	XP_005250946.1:p.Ala326=
XM_011516980.2:c.1580C=	XP_011515282.2:p.Ala527=
XM_011516981.2:c.1145C=	XP_011515283.1:p.Ala382=
XM_024447131.1:c.977C=	XP_024302899.1:p.Ala326=
NM_198488.4:c.977C=	NP_940890.3:p.Ala326=
NM_198488.5:c.977C= MANE Select	NP_940890.4:p.Ala326=