Canonical Allele Identifier: CA372469429
Gene: FAM83H HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143728644C>G , CM000670.2:g.143728644C>G GRCh38
NC_000008.10:g.144810814C>G , CM000670.1:g.144810814C>G GRCh37
NC_000008.9:g.144882802C>G NCBI36
NG_016652.1:g.10101G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000388913.4:c.817G>C MANE Select ENSP00000373565.3:p.Glu273Gln
ENST00000650760.1:c.1420G>C ENSP00000499217.1:p.Glu474Gln
ENST00000388913.3:c.817G>C ENSP00000373565.3:p.Glu273Gln
NM_198488.3:c.817G>C NP_940890.3:p.Glu273Gln
XM_005250887.2:c.874G>C XP_005250944.1:p.Glu292Gln
XM_005250888.2:c.835G>C XP_005250945.1:p.Glu279Gln
XM_005250889.2:c.817G>C XP_005250946.1:p.Glu273Gln
XM_011516980.1:c.1138G>C XP_011515282.1:p.Glu380Gln
XM_011516981.1:c.985G>C XP_011515283.1:p.Glu329Gln
XM_005250887.3:c.874G>C XP_005250944.1:p.Glu292Gln
XM_005250888.3:c.835G>C XP_005250945.1:p.Glu279Gln
XM_005250889.3:c.817G>C XP_005250946.1:p.Glu273Gln
XM_011516980.2:c.1420G>C XP_011515282.2:p.Glu474Gln
XM_011516981.2:c.985G>C XP_011515283.1:p.Glu329Gln
XM_024447131.1:c.817G>C XP_024302899.1:p.Glu273Gln
NM_198488.4:c.817G>C NP_940890.3:p.Glu273Gln
NM_198488.5:c.817G>C MANE Select NP_940890.4:p.Glu273Gln