Canonical Allele Identifier: CA1622258506

Gene: BTBD9

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.38473244A= , CM000668.2:g.38473244A=	GRCh38
NC_000006.11:g.38441020A= , CM000668.1:g.38441020A=	GRCh37
NC_000006.10:g.38548998A=	NCBI36
NG_016545.1:g.171905T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000481247.6:c.1154+104356T= MANE Select	ENSP00000418751.1:n.1154+104356T=
ENST00000649492.1:c.1154+104356T=	ENSP00000497066.1:n.1154+104356T=
ENST00000314100.10:c.950+104356T=	ENSP00000323408.6:n.950+104356T=
ENST00000328403.10:c.*62+31250T=	ENSP00000328328.6:n.*62+31250T=
ENST00000419706.6:c.978-70341T=	ENSP00000415365.2:n.978-70341T=
ENST00000481247.5:c.1154+104356T=	ENSP00000418751.1:n.1154+104356T=
NM_001099272.1:c.1154+104356T=	NP_001092742.1:n.1154+104356T=
NM_001172418.1:c.978-70341T=	NP_001165889.1:n.978-70341T=
NM_052893.1:c.1154+104356T=	NP_443125.1:n.1154+104356T=
NM_152733.2:c.950+104356T=	NP_689946.2:n.950+104356T=
XM_005248841.2:c.1154+104356T=	XP_005248898.1:n.1154+104356T=
XM_011514279.1:c.1154+104356T=	XP_011512581.1:n.1154+104356T=
XM_011514281.1:c.1154+104356T=	XP_011512583.1:n.1154+104356T=
XM_011514279.3:c.1154+104356T=	XP_011512581.1:n.1154+104356T=
XM_011514281.3:c.1154+104356T=	XP_011512583.1:n.1154+104356T=
NM_001099272.2:c.1154+104356T= MANE Select	NP_001092742.1:n.1154+104356T=
NM_052893.2:c.1154+104356T=	NP_443125.1:n.1154+104356T=
NM_001172418.2:c.978-70341T=	NP_001165889.1:n.978-70341T=
NM_152733.3:c.950+104356T=	NP_689946.2:n.950+104356T=