Canonical Allele Identifier: CA500024115
Community Standard Title: NM_021939.4(FKBP10):c.906C>A (p.Leu302=)
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41819388C>A , CM000679.2:g.41819388C>A GRCh38
NC_000017.10:g.39975640C>A , CM000679.1:g.39975640C>A GRCh37
NC_000017.9:g.37229166C>A NCBI36
NG_015860.1:g.11679C>A , LRG_12:g.11679C>A

Transcript Alleles

HGVS Amino-acid Change
NM_021939.4:c.906C>A MANE Select NP_068758.3:p.Leu302=
ENST00000321562.9:c.906C>A MANE Select ENSP00000317232.4:p.Leu302=
NM_021939.3:c.906C>A , LRG_12t1:c.906C>A NP_068758.3:p.Leu302=
ENST00000321562.8:c.906C>A ENSP00000317232.4:p.Leu302=
ENST00000455106.1:c.134C>A
ENST00000487489.1:n.519C>A
ENST00000489591.5:c.*316C>A ENSP00000466352.1:n.*316C>A
ENST00000706683.1:c.727+861C>A ENSP00000516497.1:n.727+861C>A
XM_011525099.1:c.906C>A XP_011523401.1:p.Leu302=
XM_011525099.3:c.906C>A XP_011523401.1:p.Leu302=
XM_011525100.1:c.633C>A XP_011523402.1:p.Leu211=
XM_011525100.2:c.633C>A XP_011523402.1:p.Leu211=