Canonical Allele Identifier: CA1716994037
Gene: FKBP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.73332708_73332714delinsTGAACTA , CM000669.2:g.73332708_73332714delinsTGAACTA GRCh38
NC_000007.13:g.72746711_72746717delinsTGAACTA , CM000669.1:g.72746711_72746717delinsTGAACTA GRCh37
NC_000007.12:g.72384647_72384653delinsTGAACTA NCBI36
NG_023242.2:g.9553_9559delinsTGAACTA

Transcript Alleles

HGVS Amino-acid change
ENST00000252037.5:c.588+932_588+938delinsTGAACTA MANE Select ENSP00000252037.4:n.588+932_588+938delinsTGAACTA
ENST00000648538.1:c.573+932_573+938delinsTGAACTA ENSP00000497448.1:n.573+932_573+938delinsTGAACTA
ENST00000252037.4:c.588+932_588+938delinsTGAACTA ENSP00000252037.4:n.588+932_588+938delinsTGAACTA
ENST00000413573.6:c.498+932_498+938delinsTGAACTA ENSP00000394952.2:n.498+932_498+938delinsTGAACTA
ENST00000429879.5:c.573+947_573+953delinsTGAACTA ENSP00000403908.1:n.573+947_573+953delinsTGAACTA
ENST00000431982.6:c.573+932_573+938delinsTGAACTA ENSP00000416277.2:n.573+932_573+938delinsTGAACTA
ENST00000442793.5:c.453+2356_453+2362delinsTGAACTA ENSP00000402360.1:n.453+2356_453+2362delinsTGAACTA
ENST00000445032.5:c.*667+932_*667+938delinsTGAACTA ENSP00000415891.1:n.*667+932_*667+938delinsTGAACTA
NM_001135211.2:c.573+932_573+938delinsTGAACTA NP_001128683.1:n.573+932_573+938delinsTGAACTA
NM_001281304.1:c.498+932_498+938delinsTGAACTA NP_001268233.1:n.498+932_498+938delinsTGAACTA
NM_003602.4:c.588+932_588+938delinsTGAACTA NP_003593.3:n.588+932_588+938delinsTGAACTA
XM_005250643.3:c.468+2356_468+2362delinsTGAACTA XP_005250700.1:n.468+2356_468+2362delinsTGAACTA
XM_006716152.2:c.573+947_573+953delinsTGAACTA XP_006716215.1:n.573+947_573+953delinsTGAACTA
XM_006716153.1:c.453+2356_453+2362delinsTGAACTA XP_006716216.1:n.453+2356_453+2362delinsTGAACTA
XM_011516644.1:c.588+932_588+938delinsTGAACTA XP_011514946.1:n.588+932_588+938delinsTGAACTA
NM_001362789.1:c.453+2356_453+2362delinsTGAACTA NP_001349718.1:n.453+2356_453+2362delinsTGAACTA
XM_017012741.1:c.558+947_558+953delinsTGAACTA XP_016868230.1:n.558+947_558+953delinsTGAACTA
XM_017012742.1:c.573+932_573+938delinsTGAACTA XP_016868231.1:n.573+932_573+938delinsTGAACTA
NM_003602.5:c.588+932_588+938delinsTGAACTA MANE Select NP_003593.3:n.588+932_588+938delinsTGAACTA
NM_001135211.3:c.573+932_573+938delinsTGAACTA NP_001128683.1:n.573+932_573+938delinsTGAACTA
NM_001281304.2:c.498+932_498+938delinsTGAACTA NP_001268233.1:n.498+932_498+938delinsTGAACTA
NM_001362789.2:c.453+2356_453+2362delinsTGAACTA NP_001349718.1:n.453+2356_453+2362delinsTGAACTA