Canonical Allele Identifier: CA340951931

Gene: BCL10

Linked Data

• MyVariant Identifiers: chr1:g.85736523G>T (hg19) ; chr1:g.85270840G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270840G>T , CM000663.2:g.85270840G>T	GRCh38
NC_000001.10:g.85736523G>T , CM000663.1:g.85736523G>T	GRCh37
NC_000001.9:g.85509111G>T	NCBI36
NG_012216.1:g.12061C>A
NG_012216.2:g.11065C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000620248.3:c.124C>A	ENSP00000480561.2:p.Arg42Ser
ENST00000620248.2:c.124C>A	ENSP00000480561.2:p.Arg42Ser
ENST00000648566.1:c.124C>A MANE Select	ENSP00000498104.1:p.Arg42Ser
ENST00000649060.1:c.*1233C>A	ENSP00000497490.1:n.*1233C>A
ENST00000649434.1:n.190C>A
ENST00000650582.1:n.655C>A
ENST00000370580.5:c.124C>A	ENSP00000359612.1:p.Arg42Ser
ENST00000620248.1:c.124C>A	ENSP00000480561.1:p.Arg42Ser
NM_003921.4:c.124C>A	NP_003912.1:p.Arg42Ser
XM_005271311.2:c.124C>A	XP_005271368.1:p.Arg42Ser
XM_011542397.1:c.283C>A	XP_011540699.1:p.Arg95Ser
XM_011542398.1:c.283C>A	XP_011540700.1:p.Arg95Ser
XM_011542399.1:c.70C>A	XP_011540701.1:p.Arg24Ser
NM_001320715.1:c.124C>A	NP_001307644.1:p.Arg42Ser
NM_003921.5:c.124C>A MANE Select	NP_003912.1:p.Arg42Ser
XM_011542397.3:c.283C>A	XP_011540699.1:p.Arg95Ser
XM_011542398.2:c.283C>A	XP_011540700.1:p.Arg95Ser
XM_011542399.2:c.70C>A	XP_011540701.1:p.Arg24Ser
NM_001320715.2:c.124C>A	NP_001307644.1:p.Arg42Ser