Canonical Allele Identifier: CA372468461
Gene: FAM83H HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.143728337G>C , CM000670.2:g.143728337G>C GRCh38
NC_000008.10:g.144810507G>C , CM000670.1:g.144810507G>C GRCh37
NC_000008.9:g.144882495G>C NCBI36
NG_016652.1:g.10408C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000388913.4:c.1124C>G MANE Select ENSP00000373565.3:p.Pro375Arg
ENST00000650760.1:c.1727C>G ENSP00000499217.1:p.Pro576Arg
ENST00000388913.3:c.1124C>G ENSP00000373565.3:p.Pro375Arg
ENST00000395103.2:c.304C>G
NM_198488.3:c.1124C>G NP_940890.3:p.Pro375Arg
XM_005250887.2:c.1181C>G XP_005250944.1:p.Pro394Arg
XM_005250888.2:c.1142C>G XP_005250945.1:p.Pro381Arg
XM_005250889.2:c.1124C>G XP_005250946.1:p.Pro375Arg
XM_011516980.1:c.1445C>G XP_011515282.1:p.Pro482Arg
XM_011516981.1:c.1292C>G XP_011515283.1:p.Pro431Arg
XM_005250887.3:c.1181C>G XP_005250944.1:p.Pro394Arg
XM_005250888.3:c.1142C>G XP_005250945.1:p.Pro381Arg
XM_005250889.3:c.1124C>G XP_005250946.1:p.Pro375Arg
XM_011516980.2:c.1727C>G XP_011515282.2:p.Pro576Arg
XM_011516981.2:c.1292C>G XP_011515283.1:p.Pro431Arg
XM_024447131.1:c.1124C>G XP_024302899.1:p.Pro375Arg
NM_198488.4:c.1124C>G NP_940890.3:p.Pro375Arg
NM_198488.5:c.1124C>G MANE Select NP_940890.4:p.Pro375Arg