Canonical Allele Identifier: CA418704477

Gene: BCL10

Linked Data

• gnomAD v4: 1-85270835-T-G
• MyVariant Identifiers: chr1:g.85736518T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270835T>G , CM000663.2:g.85270835T>G	GRCh38
NC_000001.10:g.85736518T>G , CM000663.1:g.85736518T>G	GRCh37
NC_000001.9:g.85509106T>G	NCBI36
NG_012216.1:g.12066A>C
NG_012216.2:g.11070A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000620248.3:c.129A>C	ENSP00000480561.2:p.Ala43=
ENST00000620248.2:c.129A>C	ENSP00000480561.2:p.Ala43=
ENST00000648566.1:c.129A>C MANE Select	ENSP00000498104.1:p.Ala43=
ENST00000649060.1:c.*1238A>C	ENSP00000497490.1:n.*1238A>C
ENST00000649434.1:n.195A>C
ENST00000650582.1:n.660A>C
ENST00000370580.5:c.129A>C	ENSP00000359612.1:p.Ala43=
ENST00000620248.1:c.129A>C	ENSP00000480561.1:p.Ala43=
NM_003921.4:c.129A>C	NP_003912.1:p.Ala43=
XM_005271311.2:c.129A>C	XP_005271368.1:p.Ala43=
XM_011542397.1:c.288A>C	XP_011540699.1:p.Ala96=
XM_011542398.1:c.288A>C	XP_011540700.1:p.Ala96=
XM_011542399.1:c.75A>C	XP_011540701.1:p.Ala25=
NM_001320715.1:c.129A>C	NP_001307644.1:p.Ala43=
NM_003921.5:c.129A>C MANE Select	NP_003912.1:p.Ala43=
XM_011542397.3:c.288A>C	XP_011540699.1:p.Ala96=
XM_011542398.2:c.288A>C	XP_011540700.1:p.Ala96=
XM_011542399.2:c.75A>C	XP_011540701.1:p.Ala25=
NM_001320715.2:c.129A>C	NP_001307644.1:p.Ala43=