Canonical Allele Identifier: CA1825940859

Gene: FAM83H

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728584G= , CM000670.2:g.143728584G=	GRCh38
NC_000008.10:g.144810754G= , CM000670.1:g.144810754G=	GRCh37
NC_000008.9:g.144882742G=	NCBI36
NG_016652.1:g.10161C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.877C= MANE Select	ENSP00000373565.3:p.Arg293=
ENST00000650760.1:c.1480C=	ENSP00000499217.1:p.Arg494=
ENST00000388913.3:c.877C=	ENSP00000373565.3:p.Arg293=
ENST00000395103.2:c.57C=
NM_198488.3:c.877C=	NP_940890.3:p.Arg293=
XM_005250887.2:c.934C=	XP_005250944.1:p.Arg312=
XM_005250888.2:c.895C=	XP_005250945.1:p.Arg299=
XM_005250889.2:c.877C=	XP_005250946.1:p.Arg293=
XM_011516980.1:c.1198C=	XP_011515282.1:p.Arg400=
XM_011516981.1:c.1045C=	XP_011515283.1:p.Arg349=
XM_005250887.3:c.934C=	XP_005250944.1:p.Arg312=
XM_005250888.3:c.895C=	XP_005250945.1:p.Arg299=
XM_005250889.3:c.877C=	XP_005250946.1:p.Arg293=
XM_011516980.2:c.1480C=	XP_011515282.2:p.Arg494=
XM_011516981.2:c.1045C=	XP_011515283.1:p.Arg349=
XM_024447131.1:c.877C=	XP_024302899.1:p.Arg293=
NM_198488.4:c.877C=	NP_940890.3:p.Arg293=
NM_198488.5:c.877C= MANE Select	NP_940890.4:p.Arg293=