Canonical Allele Identifier: CA372468910

Gene: FAM83H

Linked Data

• MyVariant Identifiers: chr8:g.144810634G>C (hg19) ; chr8:g.143728464G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.143728464G>C , CM000670.2:g.143728464G>C	GRCh38
NC_000008.10:g.144810634G>C , CM000670.1:g.144810634G>C	GRCh37
NC_000008.9:g.144882622G>C	NCBI36
NG_016652.1:g.10281C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388913.4:c.997C>G MANE Select	ENSP00000373565.3:p.Pro333Ala
ENST00000650760.1:c.1600C>G	ENSP00000499217.1:p.Pro534Ala
ENST00000388913.3:c.997C>G	ENSP00000373565.3:p.Pro333Ala
ENST00000395103.2:c.177C>G
NM_198488.3:c.997C>G	NP_940890.3:p.Pro333Ala
XM_005250887.2:c.1054C>G	XP_005250944.1:p.Pro352Ala
XM_005250888.2:c.1015C>G	XP_005250945.1:p.Pro339Ala
XM_005250889.2:c.997C>G	XP_005250946.1:p.Pro333Ala
XM_011516980.1:c.1318C>G	XP_011515282.1:p.Pro440Ala
XM_011516981.1:c.1165C>G	XP_011515283.1:p.Pro389Ala
XM_005250887.3:c.1054C>G	XP_005250944.1:p.Pro352Ala
XM_005250888.3:c.1015C>G	XP_005250945.1:p.Pro339Ala
XM_005250889.3:c.997C>G	XP_005250946.1:p.Pro333Ala
XM_011516980.2:c.1600C>G	XP_011515282.2:p.Pro534Ala
XM_011516981.2:c.1165C>G	XP_011515283.1:p.Pro389Ala
XM_024447131.1:c.997C>G	XP_024302899.1:p.Pro333Ala
NM_198488.4:c.997C>G	NP_940890.3:p.Pro333Ala
NM_198488.5:c.997C>G MANE Select	NP_940890.4:p.Pro333Ala