Canonical Allele Identifier: CA340951066

Gene: BCL10

Linked Data

• MyVariant Identifiers: chr1:g.85736330A>T (hg19) ; chr1:g.85270647A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270647A>T , CM000663.2:g.85270647A>T	GRCh38
NC_000001.10:g.85736330A>T , CM000663.1:g.85736330A>T	GRCh37
NC_000001.9:g.85508918A>T	NCBI36
NG_012216.1:g.12254T>A
NG_012216.2:g.11258T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620248.3:c.317T>A	ENSP00000480561.2:p.Leu106His
ENST00000620248.2:c.317T>A	ENSP00000480561.2:p.Leu106His
ENST00000648566.1:c.317T>A MANE Select	ENSP00000498104.1:p.Leu106His
ENST00000649434.1:n.383T>A
ENST00000650582.1:n.848T>A
ENST00000370580.5:c.317T>A	ENSP00000359612.1:p.Leu106His
ENST00000620248.1:c.317T>A	ENSP00000480561.1:p.Leu106His
NM_003921.4:c.317T>A	NP_003912.1:p.Leu106His
XM_005271311.2:c.317T>A	XP_005271368.1:p.Leu106His
XM_011542397.1:c.476T>A	XP_011540699.1:p.Leu159His
XM_011542398.1:c.476T>A	XP_011540700.1:p.Leu159His
XM_011542399.1:c.263T>A	XP_011540701.1:p.Leu88His
NM_001320715.1:c.317T>A	NP_001307644.1:p.Leu106His
NM_003921.5:c.317T>A MANE Select	NP_003912.1:p.Leu106His
XM_011542397.3:c.476T>A	XP_011540699.1:p.Leu159His
XM_011542398.2:c.476T>A	XP_011540700.1:p.Leu159His
XM_011542399.2:c.263T>A	XP_011540701.1:p.Leu88His
NM_001320715.2:c.317T>A	NP_001307644.1:p.Leu106His