Canonical Allele Identifier: CA10650104
Community Standard Title: NM_021939.4(FKBP10):c.505C>G (p.Arg169Gly)
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41818202C>G , CM000679.2:g.41818202C>G GRCh38
NC_000017.10:g.39974454C>G , CM000679.1:g.39974454C>G GRCh37
NC_000017.9:g.37227980C>G NCBI36
NG_015860.1:g.10493C>G , LRG_12:g.10493C>G

Transcript Alleles

HGVS Amino-acid Change
NM_021939.4:c.505C>G MANE Select NP_068758.3:p.Arg169Gly
ENST00000321562.9:c.505C>G MANE Select ENSP00000317232.4:p.Arg169Gly
NM_021939.3:c.505C>G , LRG_12t1:c.505C>G NP_068758.3:p.Arg169Gly
ENST00000321562.8:c.505C>G ENSP00000317232.4:p.Arg169Gly
ENST00000489591.5:c.359C>G ENSP00000466352.1:p.Pro120Arg
ENST00000585664.5:c.325C>G ENSP00000468703.1:p.Arg109Gly
ENST00000585922.5:c.505C>G ENSP00000466097.1:p.Arg169Gly
ENST00000706683.1:c.505C>G ENSP00000516497.1:p.Arg169Gly
XM_011525099.1:c.505C>G XP_011523401.1:p.Arg169Gly
XM_011525099.3:c.505C>G XP_011523401.1:p.Arg169Gly
XM_011525100.1:c.232C>G XP_011523402.1:p.Arg78Gly
XM_011525100.2:c.232C>G XP_011523402.1:p.Arg78Gly