Canonical Allele Identifier: CA1825940874

Gene: FAM83H

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728606C= , CM000670.2:g.143728606C=	GRCh38
NC_000008.10:g.144810776C= , CM000670.1:g.144810776C=	GRCh37
NC_000008.9:g.144882764C=	NCBI36
NG_016652.1:g.10139G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.855G= MANE Select	ENSP00000373565.3:p.Val285=
ENST00000650760.1:c.1458G=	ENSP00000499217.1:p.Val486=
ENST00000388913.3:c.855G=	ENSP00000373565.3:p.Val285=
ENST00000395103.2:c.35G=
NM_198488.3:c.855G=	NP_940890.3:p.Val285=
XM_005250887.2:c.912G=	XP_005250944.1:p.Val304=
XM_005250888.2:c.873G=	XP_005250945.1:p.Val291=
XM_005250889.2:c.855G=	XP_005250946.1:p.Val285=
XM_011516980.1:c.1176G=	XP_011515282.1:p.Val392=
XM_011516981.1:c.1023G=	XP_011515283.1:p.Val341=
XM_005250887.3:c.912G=	XP_005250944.1:p.Val304=
XM_005250888.3:c.873G=	XP_005250945.1:p.Val291=
XM_005250889.3:c.855G=	XP_005250946.1:p.Val285=
XM_011516980.2:c.1458G=	XP_011515282.2:p.Val486=
XM_011516981.2:c.1023G=	XP_011515283.1:p.Val341=
XM_024447131.1:c.855G=	XP_024302899.1:p.Val285=
NM_198488.4:c.855G=	NP_940890.3:p.Val285=
NM_198488.5:c.855G= MANE Select	NP_940890.4:p.Val285=