Canonical Allele Identifier: CA8566708
Community Standard Title: NM_021939.4(FKBP10):c.1613T>C (p.Met538Thr)
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41822272T>C , CM000679.2:g.41822272T>C GRCh38
NC_000017.10:g.39978524T>C , CM000679.1:g.39978524T>C GRCh37
NC_000017.9:g.37232050T>C NCBI36
NG_015860.1:g.14563T>C , LRG_12:g.14563T>C

Transcript Alleles

HGVS Amino-acid Change
NM_021939.4:c.1613T>C MANE Select NP_068758.3:p.Met538Thr
ENST00000321562.9:c.1613T>C MANE Select ENSP00000317232.4:p.Met538Thr
NM_021939.3:c.1613T>C , LRG_12t1:c.1613T>C NP_068758.3:p.Met538Thr
ENST00000321562.8:c.1613T>C ENSP00000317232.4:p.Met538Thr
ENST00000455106.1:c.1024T>C
ENST00000464180.1:n.861T>C
ENST00000489591.5:c.*1397T>C ENSP00000466352.1:n.*1397T>C
ENST00000490938.5:n.816T>C
ENST00000706683.1:c.1277T>C ENSP00000516497.1:p.Met426Thr
XM_011525099.1:c.1670T>C XP_011523401.1:p.Met557Thr
XM_011525099.3:c.1670T>C XP_011523401.1:p.Met557Thr
XM_011525100.1:c.1397T>C XP_011523402.1:p.Met466Thr
XM_011525100.2:c.1397T>C XP_011523402.1:p.Met466Thr