Canonical Allele Identifier: CA2476012568

Gene: BCL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270827_85270828delinsAT , CM000663.2:g.85270827_85270828delinsAT	GRCh38
NC_000001.10:g.85736510_85736511delinsAT , CM000663.1:g.85736510_85736511delinsAT	GRCh37
NC_000001.9:g.85509098_85509099delinsAT	NCBI36
NG_012216.1:g.12073_12074delinsAT
NG_012216.2:g.11077_11078delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000620248.3:c.136_137delinsAT	ENSP00000480561.2:p.Ile46=
ENST00000620248.2:c.136_137delinsAT	ENSP00000480561.2:p.Ile46=
ENST00000648566.1:c.136_137delinsAT MANE Select	ENSP00000498104.1:p.Ile46=
ENST00000649060.1:c.*1245_*1246delinsAT	ENSP00000497490.1:n.*1245_*1246delinsAT
ENST00000649434.1:n.202_203delinsAT
ENST00000650582.1:n.667_668delinsAT
ENST00000370580.5:c.136_137delinsAT	ENSP00000359612.1:p.Ile46=
ENST00000620248.1:c.136_137delinsAT	ENSP00000480561.1:p.Ile46=
NM_003921.4:c.136_137delinsAT	NP_003912.1:p.Ile46=
XM_005271311.2:c.136_137delinsAT	XP_005271368.1:p.Ile46=
XM_011542397.1:c.295_296delinsAT	XP_011540699.1:p.Ile99=
XM_011542398.1:c.295_296delinsAT	XP_011540700.1:p.Ile99=
XM_011542399.1:c.82_83delinsAT	XP_011540701.1:p.Ile28=
NM_001320715.1:c.136_137delinsAT	NP_001307644.1:p.Ile46=
NM_003921.5:c.136_137delinsAT MANE Select	NP_003912.1:p.Ile46=
XM_011542397.3:c.295_296delinsAT	XP_011540699.1:p.Ile99=
XM_011542398.2:c.295_296delinsAT	XP_011540700.1:p.Ile99=
XM_011542399.2:c.82_83delinsAT	XP_011540701.1:p.Ile28=
NM_001320715.2:c.136_137delinsAT	NP_001307644.1:p.Ile46=