Canonical Allele Identifier: CA399518892
Community Standard Title: NM_021939.4(FKBP10):c.1522G>A (p.Asp508Asn)
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41821776G>A , CM000679.2:g.41821776G>A GRCh38
NC_000017.10:g.39978028G>A , CM000679.1:g.39978028G>A GRCh37
NC_000017.9:g.37231554G>A NCBI36
NG_015860.1:g.14067G>A , LRG_12:g.14067G>A

Transcript Alleles

HGVS Amino-acid Change
NM_021939.4:c.1522G>A MANE Select NP_068758.3:p.Asp508Asn
ENST00000321562.9:c.1522G>A MANE Select ENSP00000317232.4:p.Asp508Asn
NM_021939.3:c.1522G>A , LRG_12t1:c.1522G>A NP_068758.3:p.Asp508Asn
ENST00000321562.8:c.1522G>A ENSP00000317232.4:p.Asp508Asn
ENST00000455106.1:c.933G>A
ENST00000464180.1:n.770G>A
ENST00000489591.5:c.*1306G>A ENSP00000466352.1:n.*1306G>A
ENST00000490938.5:n.725G>A
ENST00000706683.1:c.1186G>A ENSP00000516497.1:p.Asp396Asn
XM_011525099.1:c.1579G>A XP_011523401.1:p.Asp527Asn
XM_011525099.3:c.1579G>A XP_011523401.1:p.Asp527Asn
XM_011525100.1:c.1306G>A XP_011523402.1:p.Asp436Asn
XM_011525100.2:c.1306G>A XP_011523402.1:p.Asp436Asn