Canonical Allele Identifier: CA10639621
Community Standard Title: NM_021939.4(FKBP10):c.*422C>G
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41822830C>G , CM000679.2:g.41822830C>G GRCh38
NC_000017.10:g.39979082C>G , CM000679.1:g.39979082C>G GRCh37
NC_000017.9:g.37232608C>G NCBI36
NG_015860.1:g.15121C>G , LRG_12:g.15121C>G

Transcript Alleles

HGVS Amino-acid Change
NM_021939.4:c.*422C>G MANE Select NP_068758.3:n.*422C>G
ENST00000321562.9:c.*422C>G MANE Select ENSP00000317232.4:n.*422C>G
NM_021939.3:c.*422C>G , LRG_12t1:c.*422C>G NP_068758.3:n.*422C>G
ENST00000321562.8:c.*422C>G ENSP00000317232.4:n.*422C>G
ENST00000455106.1:c.1582C>G
ENST00000489591.5:c.*1955C>G ENSP00000466352.1:n.*1955C>G
ENST00000706683.1:c.*422C>G ENSP00000516497.1:n.*422C>G
XM_011525099.1:c.*422C>G XP_011523401.1:n.*422C>G
XM_011525099.3:c.*422C>G XP_011523401.1:n.*422C>G
XM_011525100.1:c.*422C>G XP_011523402.1:n.*422C>G
XM_011525100.2:c.*422C>G XP_011523402.1:n.*422C>G