Canonical Allele Identifier: CA463520031

Gene: FAM83H

Linked Data

• MyVariant Identifiers: chr8:g.144810782C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728612C>G , CM000670.2:g.143728612C>G	GRCh38
NC_000008.10:g.144810782C>G , CM000670.1:g.144810782C>G	GRCh37
NC_000008.9:g.144882770C>G	NCBI36
NG_016652.1:g.10133G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.849G>C MANE Select	ENSP00000373565.3:p.Pro283=
ENST00000650760.1:c.1452G>C	ENSP00000499217.1:p.Pro484=
ENST00000388913.3:c.849G>C	ENSP00000373565.3:p.Pro283=
ENST00000395103.2:c.29G>C
NM_198488.3:c.849G>C	NP_940890.3:p.Pro283=
XM_005250887.2:c.906G>C	XP_005250944.1:p.Pro302=
XM_005250888.2:c.867G>C	XP_005250945.1:p.Pro289=
XM_005250889.2:c.849G>C	XP_005250946.1:p.Pro283=
XM_011516980.1:c.1170G>C	XP_011515282.1:p.Pro390=
XM_011516981.1:c.1017G>C	XP_011515283.1:p.Pro339=
XM_005250887.3:c.906G>C	XP_005250944.1:p.Pro302=
XM_005250888.3:c.867G>C	XP_005250945.1:p.Pro289=
XM_005250889.3:c.849G>C	XP_005250946.1:p.Pro283=
XM_011516980.2:c.1452G>C	XP_011515282.2:p.Pro484=
XM_011516981.2:c.1017G>C	XP_011515283.1:p.Pro339=
XM_024447131.1:c.849G>C	XP_024302899.1:p.Pro283=
NM_198488.4:c.849G>C	NP_940890.3:p.Pro283=
NM_198488.5:c.849G>C MANE Select	NP_940890.4:p.Pro283=