Canonical Allele Identifier: CA1144228885
Gene: BCL10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.85270828_85270835delinsTTTTTTTT , CM000663.2:g.85270828_85270835delinsTTTTTTTT GRCh38
NC_000001.10:g.85736511_85736518delinsTTTTTTTT , CM000663.1:g.85736511_85736518delinsTTTTTTTT GRCh37
NC_000001.9:g.85509099_85509106delinsTTTTTTTT NCBI36
NG_012216.1:g.12066_12073delinsAAAAAAAA
NG_012216.2:g.11070_11077delinsAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000620248.3:c.129_136delinsAAAAAAAA ENSP00000480561.2:p.Ala43=
ENST00000620248.2:c.129_136delinsAAAAAAAA ENSP00000480561.2:p.Ala43=
ENST00000648566.1:c.129_136delinsAAAAAAAA MANE Select ENSP00000498104.1:p.Ala43=
ENST00000649060.1:c.*1238_*1245delinsAAAAAAAA ENSP00000497490.1:n.*1238_*1245delinsAAAAAAAA
ENST00000649434.1:n.195_202delinsAAAAAAAA
ENST00000650582.1:n.660_667delinsAAAAAAAA
ENST00000370580.5:c.129_136delinsAAAAAAAA ENSP00000359612.1:p.Ala43=
ENST00000620248.1:c.129_136delinsAAAAAAAA ENSP00000480561.1:p.Ala43=
NM_003921.4:c.129_136delinsAAAAAAAA NP_003912.1:p.Ala43=
XM_005271311.2:c.129_136delinsAAAAAAAA XP_005271368.1:p.Ala43=
XM_011542397.1:c.288_295delinsAAAAAAAA XP_011540699.1:p.Ala96=
XM_011542398.1:c.288_295delinsAAAAAAAA XP_011540700.1:p.Ala96=
XM_011542399.1:c.75_82delinsAAAAAAAA XP_011540701.1:p.Ala25=
NM_001320715.1:c.129_136delinsAAAAAAAA NP_001307644.1:p.Ala43=
NM_003921.5:c.129_136delinsAAAAAAAA MANE Select NP_003912.1:p.Ala43=
XM_011542397.3:c.288_295delinsAAAAAAAA XP_011540699.1:p.Ala96=
XM_011542398.2:c.288_295delinsAAAAAAAA XP_011540700.1:p.Ala96=
XM_011542399.2:c.75_82delinsAAAAAAAA XP_011540701.1:p.Ala25=
NM_001320715.2:c.129_136delinsAAAAAAAA NP_001307644.1:p.Ala43=