Canonical Allele Identifier: CA1716993961

Gene: FKBP6

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73332546A= , CM000669.2:g.73332546A=	GRCh38
NC_000007.13:g.72746549A= , CM000669.1:g.72746549A=	GRCh37
NC_000007.12:g.72384485A=	NCBI36
NG_023242.2:g.9391A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252037.5:c.588+770A= MANE Select	ENSP00000252037.4:n.588+770A=
ENST00000648538.1:c.573+770A=	ENSP00000497448.1:n.573+770A=
ENST00000252037.4:c.588+770A=	ENSP00000252037.4:n.588+770A=
ENST00000413573.6:c.498+770A=	ENSP00000394952.2:n.498+770A=
ENST00000429879.5:c.573+785A=	ENSP00000403908.1:n.573+785A=
ENST00000431982.6:c.573+770A=	ENSP00000416277.2:n.573+770A=
ENST00000442793.5:c.453+2194A=	ENSP00000402360.1:n.453+2194A=
ENST00000445032.5:c.*667+770A=	ENSP00000415891.1:n.*667+770A=
NM_001135211.2:c.573+770A=	NP_001128683.1:n.573+770A=
NM_001281304.1:c.498+770A=	NP_001268233.1:n.498+770A=
NM_003602.4:c.588+770A=	NP_003593.3:n.588+770A=
XM_005250643.3:c.468+2194A=	XP_005250700.1:n.468+2194A=
XM_006716152.2:c.573+785A=	XP_006716215.1:n.573+785A=
XM_006716153.1:c.453+2194A=	XP_006716216.1:n.453+2194A=
XM_011516644.1:c.588+770A=	XP_011514946.1:n.588+770A=
NM_001362789.1:c.453+2194A=	NP_001349718.1:n.453+2194A=
XM_017012741.1:c.558+785A=	XP_016868230.1:n.558+785A=
XM_017012742.1:c.573+770A=	XP_016868231.1:n.573+770A=
NM_003602.5:c.588+770A= MANE Select	NP_003593.3:n.588+770A=
NM_001135211.3:c.573+770A=	NP_001128683.1:n.573+770A=
NM_001281304.2:c.498+770A=	NP_001268233.1:n.498+770A=
NM_001362789.2:c.453+2194A=	NP_001349718.1:n.453+2194A=