Canonical Allele Identifier: CA418704355

Gene: BCL10

Linked Data

• MyVariant Identifiers: chr1:g.85736413A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270730A>C , CM000663.2:g.85270730A>C	GRCh38
NC_000001.10:g.85736413A>C , CM000663.1:g.85736413A>C	GRCh37
NC_000001.9:g.85509001A>C	NCBI36
NG_012216.1:g.12171T>G
NG_012216.2:g.11175T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000620248.3:c.234T>G	ENSP00000480561.2:p.Gly78=
ENST00000620248.2:c.234T>G	ENSP00000480561.2:p.Gly78=
ENST00000648566.1:c.234T>G MANE Select	ENSP00000498104.1:p.Gly78=
ENST00000649434.1:n.300T>G
ENST00000650582.1:n.765T>G
ENST00000370580.5:c.234T>G	ENSP00000359612.1:p.Gly78=
ENST00000620248.1:c.234T>G	ENSP00000480561.1:p.Gly78=
NM_003921.4:c.234T>G	NP_003912.1:p.Gly78=
XM_005271311.2:c.234T>G	XP_005271368.1:p.Gly78=
XM_011542397.1:c.393T>G	XP_011540699.1:p.Gly131=
XM_011542398.1:c.393T>G	XP_011540700.1:p.Gly131=
XM_011542399.1:c.180T>G	XP_011540701.1:p.Gly60=
NM_001320715.1:c.234T>G	NP_001307644.1:p.Gly78=
NM_003921.5:c.234T>G MANE Select	NP_003912.1:p.Gly78=
XM_011542397.3:c.393T>G	XP_011540699.1:p.Gly131=
XM_011542398.2:c.393T>G	XP_011540700.1:p.Gly131=
XM_011542399.2:c.180T>G	XP_011540701.1:p.Gly60=
NM_001320715.2:c.234T>G	NP_001307644.1:p.Gly78=