Canonical Allele Identifier: CA8566436
Community Standard Title: NM_021939.4(FKBP10):c.942T>C (p.Asn314=)
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41819554T>C , CM000679.2:g.41819554T>C GRCh38
NC_000017.10:g.39975806T>C , CM000679.1:g.39975806T>C GRCh37
NC_000017.9:g.37229332T>C NCBI36
NG_015860.1:g.11845T>C , LRG_12:g.11845T>C

Transcript Alleles

HGVS Amino-acid Change
NM_021939.4:c.942T>C MANE Select NP_068758.3:p.Asn314=
ENST00000321562.9:c.942T>C MANE Select ENSP00000317232.4:p.Asn314=
NM_021939.3:c.942T>C , LRG_12t1:c.942T>C NP_068758.3:p.Asn314=
ENST00000321562.8:c.942T>C ENSP00000317232.4:p.Asn314=
ENST00000455106.1:c.170T>C
ENST00000487489.1:n.555T>C
ENST00000489591.5:c.*352T>C ENSP00000466352.1:n.*352T>C
ENST00000706683.1:c.728-715T>C ENSP00000516497.1:n.728-715T>C
XM_011525099.1:c.942T>C XP_011523401.1:p.Asn314=
XM_011525099.3:c.942T>C XP_011523401.1:p.Asn314=
XM_011525100.1:c.669T>C XP_011523402.1:p.Asn223=
XM_011525100.2:c.669T>C XP_011523402.1:p.Asn223=