Canonical Allele Identifier: CA340951520

Gene: BCL10

Linked Data

• MyVariant Identifiers: chr1:g.85736420G>A (hg19) ; chr1:g.85270737G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.85270737G>A , CM000663.2:g.85270737G>A	GRCh38
NC_000001.10:g.85736420G>A , CM000663.1:g.85736420G>A	GRCh37
NC_000001.9:g.85509008G>A	NCBI36
NG_012216.1:g.12164C>T
NG_012216.2:g.11168C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000620248.3:c.227C>T	ENSP00000480561.2:p.Pro76Leu
ENST00000620248.2:c.227C>T	ENSP00000480561.2:p.Pro76Leu
ENST00000648566.1:c.227C>T MANE Select	ENSP00000498104.1:p.Pro76Leu
ENST00000649434.1:n.293C>T
ENST00000650582.1:n.758C>T
ENST00000370580.5:c.227C>T	ENSP00000359612.1:p.Pro76Leu
ENST00000620248.1:c.227C>T	ENSP00000480561.1:p.Pro76Leu
NM_003921.4:c.227C>T	NP_003912.1:p.Pro76Leu
XM_005271311.2:c.227C>T	XP_005271368.1:p.Pro76Leu
XM_011542397.1:c.386C>T	XP_011540699.1:p.Pro129Leu
XM_011542398.1:c.386C>T	XP_011540700.1:p.Pro129Leu
XM_011542399.1:c.173C>T	XP_011540701.1:p.Pro58Leu
NM_001320715.1:c.227C>T	NP_001307644.1:p.Pro76Leu
NM_003921.5:c.227C>T MANE Select	NP_003912.1:p.Pro76Leu
XM_011542397.3:c.386C>T	XP_011540699.1:p.Pro129Leu
XM_011542398.2:c.386C>T	XP_011540700.1:p.Pro129Leu
XM_011542399.2:c.173C>T	XP_011540701.1:p.Pro58Leu
NM_001320715.2:c.227C>T	NP_001307644.1:p.Pro76Leu