Canonical Allele Identifier: CA418704232

Gene: BCL10

Linked Data

• gnomAD v4: 1-85270643-T-C
• MyVariant Identifiers: chr1:g.85736326T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270643T>C , CM000663.2:g.85270643T>C	GRCh38
NC_000001.10:g.85736326T>C , CM000663.1:g.85736326T>C	GRCh37
NC_000001.9:g.85508914T>C	NCBI36
NG_012216.1:g.12258A>G
NG_012216.2:g.11262A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000620248.3:c.321A>G	ENSP00000480561.2:p.Arg107=
ENST00000620248.2:c.321A>G	ENSP00000480561.2:p.Arg107=
ENST00000648566.1:c.321A>G MANE Select	ENSP00000498104.1:p.Arg107=
ENST00000649434.1:n.387A>G
ENST00000650582.1:n.852A>G
ENST00000370580.5:c.321A>G	ENSP00000359612.1:p.Arg107=
ENST00000620248.1:c.321A>G	ENSP00000480561.1:p.Arg107=
NM_003921.4:c.321A>G	NP_003912.1:p.Arg107=
XM_005271311.2:c.321A>G	XP_005271368.1:p.Arg107=
XM_011542397.1:c.480A>G	XP_011540699.1:p.Arg160=
XM_011542398.1:c.480A>G	XP_011540700.1:p.Arg160=
XM_011542399.1:c.267A>G	XP_011540701.1:p.Arg89=
NM_001320715.1:c.321A>G	NP_001307644.1:p.Arg107=
NM_003921.5:c.321A>G MANE Select	NP_003912.1:p.Arg107=
XM_011542397.3:c.480A>G	XP_011540699.1:p.Arg160=
XM_011542398.2:c.480A>G	XP_011540700.1:p.Arg160=
XM_011542399.2:c.267A>G	XP_011540701.1:p.Arg89=
NM_001320715.2:c.321A>G	NP_001307644.1:p.Arg107=