Canonical Allele Identifier: CA8566710
Community Standard Title: NM_021939.4(FKBP10):c.1621C>T (p.Gln541Ter)
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41822280C>T , CM000679.2:g.41822280C>T GRCh38
NC_000017.10:g.39978532C>T , CM000679.1:g.39978532C>T GRCh37
NC_000017.9:g.37232058C>T NCBI36
NG_015860.1:g.14571C>T , LRG_12:g.14571C>T

Transcript Alleles

HGVS Amino-acid Change
NM_021939.4:c.1621C>T MANE Select NP_068758.3:p.Gln541Ter
ENST00000321562.9:c.1621C>T MANE Select ENSP00000317232.4:p.Gln541Ter
NM_021939.3:c.1621C>T , LRG_12t1:c.1621C>T NP_068758.3:p.Gln541Ter
ENST00000321562.8:c.1621C>T ENSP00000317232.4:p.Gln541Ter
ENST00000455106.1:c.1032C>T
ENST00000464180.1:n.869C>T
ENST00000489591.5:c.*1405C>T ENSP00000466352.1:n.*1405C>T
ENST00000490938.5:n.824C>T
ENST00000706683.1:c.1285C>T ENSP00000516497.1:p.Gln429Ter
XM_011525099.1:c.1678C>T XP_011523401.1:p.Gln560Ter
XM_011525099.3:c.1678C>T XP_011523401.1:p.Gln560Ter
XM_011525100.1:c.1405C>T XP_011523402.1:p.Gln469Ter
XM_011525100.2:c.1405C>T XP_011523402.1:p.Gln469Ter