Canonical Allele Identifier: CA173958

Gene: BCL10

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85276295C>T , CM000663.2:g.85276295C>T	GRCh38
NC_000001.10:g.85741978C>T , CM000663.1:g.85741978C>T	GRCh37
NC_000001.9:g.85514566C>T	NCBI36
NG_012216.1:g.6606G>A
NG_012216.2:g.5610G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003921.5:c.57+1G>A MANE Select	NP_003912.1:n.57+1G>A
ENST00000648566.1:c.57+1G>A MANE Select	ENSP00000498104.1:n.57+1G>A
NM_001320715.1:c.57+1G>A	NP_001307644.1:n.57+1G>A
NM_001320715.2:c.57+1G>A	NP_001307644.1:n.57+1G>A
NM_003921.4:c.57+1G>A	NP_003912.1:n.57+1G>A
ENST00000370580.5:c.57+1G>A	ENSP00000359612.1:n.57+1G>A
ENST00000620248.1:c.57+1G>A	ENSP00000480561.1:n.57+1G>A
ENST00000620248.2:c.57+1G>A	ENSP00000480561.2:n.57+1G>A
ENST00000620248.3:c.57+1G>A	ENSP00000480561.2:n.57+1G>A
ENST00000649060.1:c.58G>A	ENSP00000497490.1:p.Val20Met
ENST00000649434.1:n.123+1G>A
XM_005271311.2:c.57+1G>A	XP_005271368.1:n.57+1G>A