Canonical Allele Identifier: CA8566716
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41822299T>C , CM000679.2:g.41822299T>C GRCh38
NC_000017.10:g.39978551T>C , CM000679.1:g.39978551T>C GRCh37
NC_000017.9:g.37232077T>C NCBI36
NG_015860.1:g.14590T>C , LRG_12:g.14590T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706683.1:c.1304T>C ENSP00000516497.1:p.Ile435Thr
ENST00000321562.9:c.1640T>C MANE Select ENSP00000317232.4:p.Ile547Thr
ENST00000321562.8:c.1640T>C ENSP00000317232.4:p.Ile547Thr
ENST00000455106.1:c.1051T>C
ENST00000464180.1:n.888T>C
ENST00000489591.5:c.*1424T>C ENSP00000466352.1:n.*1424T>C
NM_021939.3:c.1640T>C , LRG_12t1:c.1640T>C NP_068758.3:p.Ile547Thr
XM_011525099.1:c.1697T>C XP_011523401.1:p.Ile566Thr
XM_011525100.1:c.1424T>C XP_011523402.1:p.Ile475Thr
XM_011525099.3:c.1697T>C XP_011523401.1:p.Ile566Thr
XM_011525100.2:c.1424T>C XP_011523402.1:p.Ile475Thr
NM_021939.4:c.1640T>C MANE Select NP_068758.3:p.Ile547Thr