Canonical Allele Identifier: CA8566733
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41822393C>T , CM000679.2:g.41822393C>T GRCh38
NC_000017.10:g.39978645C>T , CM000679.1:g.39978645C>T GRCh37
NC_000017.9:g.37232171C>T NCBI36
NG_015860.1:g.14684C>T , LRG_12:g.14684C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706683.1:c.1398C>T ENSP00000516497.1:p.Val466=
ENST00000321562.9:c.1734C>T MANE Select ENSP00000317232.4:p.Val578=
ENST00000321562.8:c.1734C>T ENSP00000317232.4:p.Val578=
ENST00000455106.1:c.1145C>T
ENST00000464180.1:n.982C>T
ENST00000489591.5:c.*1518C>T ENSP00000466352.1:n.*1518C>T
NM_021939.3:c.1734C>T , LRG_12t1:c.1734C>T NP_068758.3:p.Val578=
XM_011525099.1:c.1791C>T XP_011523401.1:p.Val597=
XM_011525100.1:c.1518C>T XP_011523402.1:p.Val506=
XM_011525099.3:c.1791C>T XP_011523401.1:p.Val597=
XM_011525100.2:c.1518C>T XP_011523402.1:p.Val506=
NM_021939.4:c.1734C>T MANE Select NP_068758.3:p.Val578=