Canonical Allele Identifier: CA1825940765

Gene: FAM83H

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728420G= , CM000670.2:g.143728420G=	GRCh38
NC_000008.10:g.144810590G= , CM000670.1:g.144810590G=	GRCh37
NC_000008.9:g.144882578G=	NCBI36
NG_016652.1:g.10325C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.1041C= MANE Select	ENSP00000373565.3:p.Asp347=
ENST00000650760.1:c.1644C=	ENSP00000499217.1:p.Asp548=
ENST00000388913.3:c.1041C=	ENSP00000373565.3:p.Asp347=
ENST00000395103.2:c.221C=
NM_198488.3:c.1041C=	NP_940890.3:p.Asp347=
XM_005250887.2:c.1098C=	XP_005250944.1:p.Asp366=
XM_005250888.2:c.1059C=	XP_005250945.1:p.Asp353=
XM_005250889.2:c.1041C=	XP_005250946.1:p.Asp347=
XM_011516980.1:c.1362C=	XP_011515282.1:p.Asp454=
XM_011516981.1:c.1209C=	XP_011515283.1:p.Asp403=
XM_005250887.3:c.1098C=	XP_005250944.1:p.Asp366=
XM_005250888.3:c.1059C=	XP_005250945.1:p.Asp353=
XM_005250889.3:c.1041C=	XP_005250946.1:p.Asp347=
XM_011516980.2:c.1644C=	XP_011515282.2:p.Asp548=
XM_011516981.2:c.1209C=	XP_011515283.1:p.Asp403=
XM_024447131.1:c.1041C=	XP_024302899.1:p.Asp347=
NM_198488.4:c.1041C=	NP_940890.3:p.Asp347=
NM_198488.5:c.1041C= MANE Select	NP_940890.4:p.Asp347=