Canonical Allele Identifier: CA340951493

Gene: BCL10

Linked Data

• MyVariant Identifiers: chr1:g.85736414C>G (hg19) ; chr1:g.85270731C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270731C>G , CM000663.2:g.85270731C>G	GRCh38
NC_000001.10:g.85736414C>G , CM000663.1:g.85736414C>G	GRCh37
NC_000001.9:g.85509002C>G	NCBI36
NG_012216.1:g.12170G>C
NG_012216.2:g.11174G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000620248.3:c.233G>C	ENSP00000480561.2:p.Gly78Ala
ENST00000620248.2:c.233G>C	ENSP00000480561.2:p.Gly78Ala
ENST00000648566.1:c.233G>C MANE Select	ENSP00000498104.1:p.Gly78Ala
ENST00000649434.1:n.299G>C
ENST00000650582.1:n.764G>C
ENST00000370580.5:c.233G>C	ENSP00000359612.1:p.Gly78Ala
ENST00000620248.1:c.233G>C	ENSP00000480561.1:p.Gly78Ala
NM_003921.4:c.233G>C	NP_003912.1:p.Gly78Ala
XM_005271311.2:c.233G>C	XP_005271368.1:p.Gly78Ala
XM_011542397.1:c.392G>C	XP_011540699.1:p.Gly131Ala
XM_011542398.1:c.392G>C	XP_011540700.1:p.Gly131Ala
XM_011542399.1:c.179G>C	XP_011540701.1:p.Gly60Ala
NM_001320715.1:c.233G>C	NP_001307644.1:p.Gly78Ala
NM_003921.5:c.233G>C MANE Select	NP_003912.1:p.Gly78Ala
XM_011542397.3:c.392G>C	XP_011540699.1:p.Gly131Ala
XM_011542398.2:c.392G>C	XP_011540700.1:p.Gly131Ala
XM_011542399.2:c.179G>C	XP_011540701.1:p.Gly60Ala
NM_001320715.2:c.233G>C	NP_001307644.1:p.Gly78Ala