Canonical Allele Identifier: CA1825940845

Gene: FAM83H

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728556T= , CM000670.2:g.143728556T=	GRCh38
NC_000008.10:g.144810726T= , CM000670.1:g.144810726T=	GRCh37
NC_000008.9:g.144882714T=	NCBI36
NG_016652.1:g.10189A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.905A= MANE Select	ENSP00000373565.3:p.Tyr302=
ENST00000650760.1:c.1508A=	ENSP00000499217.1:p.Tyr503=
ENST00000388913.3:c.905A=	ENSP00000373565.3:p.Tyr302=
ENST00000395103.2:c.85A=
NM_198488.3:c.905A=	NP_940890.3:p.Tyr302=
XM_005250887.2:c.962A=	XP_005250944.1:p.Tyr321=
XM_005250888.2:c.923A=	XP_005250945.1:p.Tyr308=
XM_005250889.2:c.905A=	XP_005250946.1:p.Tyr302=
XM_011516980.1:c.1226A=	XP_011515282.1:p.Tyr409=
XM_011516981.1:c.1073A=	XP_011515283.1:p.Tyr358=
XM_005250887.3:c.962A=	XP_005250944.1:p.Tyr321=
XM_005250888.3:c.923A=	XP_005250945.1:p.Tyr308=
XM_005250889.3:c.905A=	XP_005250946.1:p.Tyr302=
XM_011516980.2:c.1508A=	XP_011515282.2:p.Tyr503=
XM_011516981.2:c.1073A=	XP_011515283.1:p.Tyr358=
XM_024447131.1:c.905A=	XP_024302899.1:p.Tyr302=
NM_198488.4:c.905A=	NP_940890.3:p.Tyr302=
NM_198488.5:c.905A= MANE Select	NP_940890.4:p.Tyr302=