Canonical Allele Identifier: CA1139997661

Gene: BCL9

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.147620166C= , CM000663.2:g.147620166C=	GRCh38
NC_000001.10:g.147091972C= , CM000663.1:g.147091972C=	GRCh37
NC_000001.9:g.145558596C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683836.1:c.2011C=	ENSP00000506908.1:p.Pro671=
ENST00000684121.1:c.1789C=	ENSP00000507238.1:p.Pro597=
ENST00000234739.8:c.2011C= MANE Select	ENSP00000234739.3:p.Pro671=
ENST00000234739.7:c.2011C=	ENSP00000234739.3:p.Pro671=
ENST00000622552.4:c.2011C=	ENSP00000479694.1:p.Pro671=
NM_004326.3:c.2011C=	NP_004317.2:p.Pro671=
XM_005272971.3:c.2011C=	XP_005273028.1:p.Pro671=
XM_005277417.2:c.2011C=	XP_005277474.1:p.Pro671=
XM_005277418.2:c.1789C=	XP_005277475.1:p.Pro597=
XM_006711483.2:c.2011C=	XP_006711546.1:p.Pro671=
XM_005272971.4:c.2011C=	XP_005273028.1:p.Pro671=
XM_005277417.4:c.2011C=	XP_005277474.1:p.Pro671=
XM_005277418.4:c.1789C=	XP_005277475.1:p.Pro597=
XM_017002026.1:c.1789C=	XP_016857515.1:p.Pro597=
NM_004326.4:c.2011C= MANE Select	NP_004317.2:p.Pro671=