Canonical Allele Identifier: CA1139665525
Community Standard Title: NM_021939.4(FKBP10):c.*197T>A
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41822605T>A , CM000679.2:g.41822605T>A GRCh38
NC_000017.10:g.39978857T>A , CM000679.1:g.39978857T>A GRCh37
NC_000017.9:g.37232383T>A NCBI36
NG_015860.1:g.14896T>A , LRG_12:g.14896T>A

Transcript Alleles

HGVS Amino-acid Change
NM_021939.4:c.*197T>A MANE Select NP_068758.3:n.*197T>A
ENST00000321562.9:c.*197T>A MANE Select ENSP00000317232.4:n.*197T>A
NM_021939.3:c.*197T>A , LRG_12t1:c.*197T>A NP_068758.3:n.*197T>A
ENST00000321562.8:c.*197T>A ENSP00000317232.4:n.*197T>A
ENST00000455106.1:c.1357T>A
ENST00000489591.5:c.*1730T>A ENSP00000466352.1:n.*1730T>A
ENST00000706683.1:c.*197T>A ENSP00000516497.1:n.*197T>A
XM_011525099.1:c.*197T>A XP_011523401.1:n.*197T>A
XM_011525099.3:c.*197T>A XP_011523401.1:n.*197T>A
XM_011525100.1:c.*197T>A XP_011523402.1:n.*197T>A
XM_011525100.2:c.*197T>A XP_011523402.1:n.*197T>A