Canonical Allele Identifier: CA1825940796

Gene: FAM83H

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728481T= , CM000670.2:g.143728481T=	GRCh38
NC_000008.10:g.144810651T= , CM000670.1:g.144810651T=	GRCh37
NC_000008.9:g.144882639T=	NCBI36
NG_016652.1:g.10264A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.980A= MANE Select	ENSP00000373565.3:p.His327=
ENST00000650760.1:c.1583A=	ENSP00000499217.1:p.His528=
ENST00000388913.3:c.980A=	ENSP00000373565.3:p.His327=
ENST00000395103.2:c.160A=
NM_198488.3:c.980A=	NP_940890.3:p.His327=
XM_005250887.2:c.1037A=	XP_005250944.1:p.His346=
XM_005250888.2:c.998A=	XP_005250945.1:p.His333=
XM_005250889.2:c.980A=	XP_005250946.1:p.His327=
XM_011516980.1:c.1301A=	XP_011515282.1:p.His434=
XM_011516981.1:c.1148A=	XP_011515283.1:p.His383=
XM_005250887.3:c.1037A=	XP_005250944.1:p.His346=
XM_005250888.3:c.998A=	XP_005250945.1:p.His333=
XM_005250889.3:c.980A=	XP_005250946.1:p.His327=
XM_011516980.2:c.1583A=	XP_011515282.2:p.His528=
XM_011516981.2:c.1148A=	XP_011515283.1:p.His383=
XM_024447131.1:c.980A=	XP_024302899.1:p.His327=
NM_198488.4:c.980A=	NP_940890.3:p.His327=
NM_198488.5:c.980A= MANE Select	NP_940890.4:p.His327=