Canonical Allele Identifier: CA8566623
Community Standard Title: NM_021939.4(FKBP10):c.1363A>G (p.Ile455Val)
Gene: FKBP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41821053A>G , CM000679.2:g.41821053A>G GRCh38
NC_000017.10:g.39977305A>G , CM000679.1:g.39977305A>G GRCh37
NC_000017.9:g.37230831A>G NCBI36
NG_015860.1:g.13344A>G , LRG_12:g.13344A>G

Transcript Alleles

HGVS Amino-acid Change
NM_021939.4:c.1363A>G MANE Select NP_068758.3:p.Ile455Val
ENST00000321562.9:c.1363A>G MANE Select ENSP00000317232.4:p.Ile455Val
NM_021939.3:c.1363A>G , LRG_12t1:c.1363A>G NP_068758.3:p.Ile455Val
ENST00000321562.8:c.1363A>G ENSP00000317232.4:p.Ile455Val
ENST00000455106.1:c.774A>G
ENST00000464180.1:n.611A>G
ENST00000489591.5:c.*1147A>G ENSP00000466352.1:n.*1147A>G
ENST00000490938.5:n.566A>G
ENST00000706683.1:c.1027A>G ENSP00000516497.1:p.Ile343Val
XM_011525099.1:c.1420A>G XP_011523401.1:p.Ile474Val
XM_011525099.3:c.1420A>G XP_011523401.1:p.Ile474Val
XM_011525100.1:c.1147A>G XP_011523402.1:p.Ile383Val
XM_011525100.2:c.1147A>G XP_011523402.1:p.Ile383Val