Canonical Allele Identifier: CA2034390335

Gene: HDAC7

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.47814541A= , CM000674.2:g.47814541A=	GRCh38
NC_000012.11:g.48208324A= , CM000674.1:g.48208324A=	GRCh37
NC_000012.10:g.46494591A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000080059.12:c.19+5226T= MANE Select	ENSP00000080059.7:n.19+5226T=
ENST00000080059.11:c.19+5226T=	ENSP00000080059.7:n.19+5226T=
ENST00000354334.7:c.19+5226T=	ENSP00000351326.3:n.19+5226T=
ENST00000417107.5:c.-99+4579T=	ENSP00000387792.1:n.-99+4579T=
ENST00000417902.5:c.19+5226T=	ENSP00000400811.1:n.19+5226T=
ENST00000425451.2:c.19+5226T=	ENSP00000401872.2:n.19+5226T=
ENST00000427332.6:c.-99+6013T=	ENSP00000404394.2:n.-99+6013T=
ENST00000430670.5:c.19+5226T=	ENSP00000396159.1:n.19+5226T=
ENST00000433685.5:c.-48+5942T=	ENSP00000403149.1:n.-48+5942T=
ENST00000434070.5:c.-98-12267T=	ENSP00000388561.1:n.-98-12267T=
ENST00000440293.5:c.19+5226T=	ENSP00000411058.1:n.19+5226T=
ENST00000447463.5:c.-48+6013T=	ENSP00000389501.2:n.-48+6013T=
ENST00000450805.5:c.-99+4579T=	ENSP00000397236.1:n.-99+4579T=
ENST00000552960.5:c.19+5226T=	ENSP00000448532.1:n.19+5226T=
NM_001098416.2:c.19+5226T=	NP_001091886.1:n.19+5226T=
NM_001098416.3:c.19+5226T=	NP_001091886.1:n.19+5226T=
NM_001308090.1:c.19+5226T=	NP_001295019.1:n.19+5226T=
NM_015401.3:c.19+5226T=	NP_056216.2:n.19+5226T=
NM_015401.4:c.19+5226T=	NP_056216.2:n.19+5226T=
XM_006719454.2:c.61+5815T=	XP_006719517.1:n.61+5815T=
XM_011538479.1:c.40+94T=	XP_011536781.1:n.40+94T=
XM_011538481.1:c.-99+6013T=	XP_011536783.1:n.-99+6013T=
XM_011538482.1:c.-99+4579T=	XP_011536784.1:n.-99+4579T=
XM_024449018.1:c.40+94T=	XP_024304786.1:n.40+94T=
NM_015401.5:c.19+5226T= MANE Select	NP_056216.2:n.19+5226T=
NM_001098416.4:c.19+5226T=	NP_001091886.1:n.19+5226T=
NM_001308090.2:c.19+5226T=	NP_001295019.1:n.19+5226T=
NM_001368046.1:c.19+5226T=	NP_001354975.1:n.19+5226T=
NR_160435.1:n.137+5226T=
NR_160436.1:n.137+5226T=