Canonical Allele Identifier: CA160057228

Gene: FKBP6

Linked Data

• dbSNP Id: rs781939907
• MyVariant Identifiers: chr7:g.72746700_72746701insTTTGTT (hg19) ; chr7:g.73332697_73332698insTTTGTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73332698_73332699insTTGTTT , CM000669.2:g.73332698_73332699insTTGTTT	GRCh38
NC_000007.13:g.72746701_72746702insTTGTTT , CM000669.1:g.72746701_72746702insTTGTTT	GRCh37
NC_000007.12:g.72384637_72384638insTTGTTT	NCBI36
NG_023242.2:g.9543_9544insTTGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252037.5:c.588+922_588+923insTTGTTT MANE Select	ENSP00000252037.4:n.588+922_588+923insTTGTTT
ENST00000648538.1:c.573+922_573+923insTTGTTT	ENSP00000497448.1:n.573+922_573+923insTTGTTT
ENST00000252037.4:c.588+922_588+923insTTGTTT	ENSP00000252037.4:n.588+922_588+923insTTGTTT
ENST00000413573.6:c.498+922_498+923insTTGTTT	ENSP00000394952.2:n.498+922_498+923insTTGTTT
ENST00000429879.5:c.573+937_573+938insTTGTTT	ENSP00000403908.1:n.573+937_573+938insTTGTTT
ENST00000431982.6:c.573+922_573+923insTTGTTT	ENSP00000416277.2:n.573+922_573+923insTTGTTT
ENST00000442793.5:c.453+2346_453+2347insTTGTTT	ENSP00000402360.1:n.453+2346_453+2347insTTGTTT
ENST00000445032.5:c.*667+922_*667+923insTTGTTT	ENSP00000415891.1:n.*667+922_*667+923insTTGTTT
NM_001135211.2:c.573+922_573+923insTTGTTT	NP_001128683.1:n.573+922_573+923insTTGTTT
NM_001281304.1:c.498+922_498+923insTTGTTT	NP_001268233.1:n.498+922_498+923insTTGTTT
NM_003602.4:c.588+922_588+923insTTGTTT	NP_003593.3:n.588+922_588+923insTTGTTT
XM_005250643.3:c.468+2346_468+2347insTTGTTT	XP_005250700.1:n.468+2346_468+2347insTTGTTT
XM_006716152.2:c.573+937_573+938insTTGTTT	XP_006716215.1:n.573+937_573+938insTTGTTT
XM_006716153.1:c.453+2346_453+2347insTTGTTT	XP_006716216.1:n.453+2346_453+2347insTTGTTT
XM_011516644.1:c.588+922_588+923insTTGTTT	XP_011514946.1:n.588+922_588+923insTTGTTT
NM_001362789.1:c.453+2346_453+2347insTTGTTT	NP_001349718.1:n.453+2346_453+2347insTTGTTT
XM_017012741.1:c.558+937_558+938insTTGTTT	XP_016868230.1:n.558+937_558+938insTTGTTT
XM_017012742.1:c.573+922_573+923insTTGTTT	XP_016868231.1:n.573+922_573+923insTTGTTT
NM_003602.5:c.588+922_588+923insTTGTTT MANE Select	NP_003593.3:n.588+922_588+923insTTGTTT
NM_001135211.3:c.573+922_573+923insTTGTTT	NP_001128683.1:n.573+922_573+923insTTGTTT
NM_001281304.2:c.498+922_498+923insTTGTTT	NP_001268233.1:n.498+922_498+923insTTGTTT
NM_001362789.2:c.453+2346_453+2347insTTGTTT	NP_001349718.1:n.453+2346_453+2347insTTGTTT