Canonical Allele Identifier: CA372469369
Gene: FAM83H HGNC NCBI

Linked Data

dbSNP Id: rs1818400607

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143728617C>T , CM000670.2:g.143728617C>T GRCh38
NC_000008.10:g.144810787C>T , CM000670.1:g.144810787C>T GRCh37
NC_000008.9:g.144882775C>T NCBI36
NG_016652.1:g.10128G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000388913.4:c.844G>A MANE Select ENSP00000373565.3:p.Glu282Lys
ENST00000650760.1:c.1447G>A ENSP00000499217.1:p.Glu483Lys
ENST00000388913.3:c.844G>A ENSP00000373565.3:p.Glu282Lys
ENST00000395103.2:c.24G>A
NM_198488.3:c.844G>A NP_940890.3:p.Glu282Lys
XM_005250887.2:c.901G>A XP_005250944.1:p.Glu301Lys
XM_005250888.2:c.862G>A XP_005250945.1:p.Glu288Lys
XM_005250889.2:c.844G>A XP_005250946.1:p.Glu282Lys
XM_011516980.1:c.1165G>A XP_011515282.1:p.Glu389Lys
XM_011516981.1:c.1012G>A XP_011515283.1:p.Glu338Lys
XM_005250887.3:c.901G>A XP_005250944.1:p.Glu301Lys
XM_005250888.3:c.862G>A XP_005250945.1:p.Glu288Lys
XM_005250889.3:c.844G>A XP_005250946.1:p.Glu282Lys
XM_011516980.2:c.1447G>A XP_011515282.2:p.Glu483Lys
XM_011516981.2:c.1012G>A XP_011515283.1:p.Glu338Lys
XM_024447131.1:c.844G>A XP_024302899.1:p.Glu282Lys
NM_198488.4:c.844G>A NP_940890.3:p.Glu282Lys
NM_198488.5:c.844G>A MANE Select NP_940890.4:p.Glu282Lys