Canonical Allele Identifier: CA4917562
Gene: FAM83H HGNC NCBI

Linked Data

dbSNP Id: rs782754851

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143728575C>T , CM000670.2:g.143728575C>T GRCh38
NC_000008.10:g.144810745C>T , CM000670.1:g.144810745C>T GRCh37
NC_000008.9:g.144882733C>T NCBI36
NG_016652.1:g.10170G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000388913.4:c.886G>A MANE Select ENSP00000373565.3:p.Ala296Thr
ENST00000650760.1:c.1489G>A ENSP00000499217.1:p.Ala497Thr
ENST00000388913.3:c.886G>A ENSP00000373565.3:p.Ala296Thr
ENST00000395103.2:c.66G>A
NM_198488.3:c.886G>A NP_940890.3:p.Ala296Thr
XM_005250887.2:c.943G>A XP_005250944.1:p.Ala315Thr
XM_005250888.2:c.904G>A XP_005250945.1:p.Ala302Thr
XM_005250889.2:c.886G>A XP_005250946.1:p.Ala296Thr
XM_011516980.1:c.1207G>A XP_011515282.1:p.Ala403Thr
XM_011516981.1:c.1054G>A XP_011515283.1:p.Ala352Thr
XM_005250887.3:c.943G>A XP_005250944.1:p.Ala315Thr
XM_005250888.3:c.904G>A XP_005250945.1:p.Ala302Thr
XM_005250889.3:c.886G>A XP_005250946.1:p.Ala296Thr
XM_011516980.2:c.1489G>A XP_011515282.2:p.Ala497Thr
XM_011516981.2:c.1054G>A XP_011515283.1:p.Ala352Thr
XM_024447131.1:c.886G>A XP_024302899.1:p.Ala296Thr
NM_198488.4:c.886G>A NP_940890.3:p.Ala296Thr
NM_198488.5:c.886G>A MANE Select NP_940890.4:p.Ala296Thr