Canonical Allele Identifier: CA1103000888
Gene: FKBP6 HGNC NCBI

Linked Data

dbSNP Id: rs1804885425
gnomAD v3: 7-73332680-G-A
gnomAD v4: 7-73332680-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73332680G>A , CM000669.2:g.73332680G>A GRCh38
NC_000007.13:g.72746683G>A , CM000669.1:g.72746683G>A GRCh37
NC_000007.12:g.72384619G>A NCBI36
NG_023242.2:g.9525G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252037.5:c.588+904G>A MANE Select ENSP00000252037.4:n.588+904G>A
ENST00000648538.1:c.573+904G>A ENSP00000497448.1:n.573+904G>A
ENST00000252037.4:c.588+904G>A ENSP00000252037.4:n.588+904G>A
ENST00000413573.6:c.498+904G>A ENSP00000394952.2:n.498+904G>A
ENST00000429879.5:c.573+919G>A ENSP00000403908.1:n.573+919G>A
ENST00000431982.6:c.573+904G>A ENSP00000416277.2:n.573+904G>A
ENST00000442793.5:c.453+2328G>A ENSP00000402360.1:n.453+2328G>A
ENST00000445032.5:c.*667+904G>A ENSP00000415891.1:n.*667+904G>A
NM_001135211.2:c.573+904G>A NP_001128683.1:n.573+904G>A
NM_001281304.1:c.498+904G>A NP_001268233.1:n.498+904G>A
NM_003602.4:c.588+904G>A NP_003593.3:n.588+904G>A
XM_005250643.3:c.468+2328G>A XP_005250700.1:n.468+2328G>A
XM_006716152.2:c.573+919G>A XP_006716215.1:n.573+919G>A
XM_006716153.1:c.453+2328G>A XP_006716216.1:n.453+2328G>A
XM_011516644.1:c.588+904G>A XP_011514946.1:n.588+904G>A
NM_001362789.1:c.453+2328G>A NP_001349718.1:n.453+2328G>A
XM_017012741.1:c.558+919G>A XP_016868230.1:n.558+919G>A
XM_017012742.1:c.573+904G>A XP_016868231.1:n.573+904G>A
NM_003602.5:c.588+904G>A MANE Select NP_003593.3:n.588+904G>A
NM_001135211.3:c.573+904G>A NP_001128683.1:n.573+904G>A
NM_001281304.2:c.498+904G>A NP_001268233.1:n.498+904G>A
NM_001362789.2:c.453+2328G>A NP_001349718.1:n.453+2328G>A