Canonical Allele Identifier: CA49021233

Gene: BCL11A

Linked Data

• dbSNP Id: rs778268980
• MyVariant Identifiers: chr2:g.60720095_60720096insG (hg19) ; chr2:g.60492960_60492961insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.60492960_60492961insG , CM000664.2:g.60492960_60492961insG	GRCh38
NC_000002.11:g.60720095_60720096insG , CM000664.1:g.60720095_60720096insG	GRCh37
NC_000002.10:g.60573599_60573600insG	NCBI36
NG_011968.1:g.65538_65539insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000335712.11:c.386-30537_386-30536insC	ENSP00000338774.7:n.386-30537_386-30536insC
ENST00000356842.9:c.386-24128_386-24127insC	ENSP00000349300.4:n.386-24128_386-24127insC
ENST00000358510.6:c.386-30537_386-30536insC	ENSP00000351307.5:n.386-30537_386-30536insC
ENST00000359629.10:c.386-24128_386-24127insC	ENSP00000352648.5:n.386-24128_386-24127insC
ENST00000489516.7:c.380-24128_380-24127insC	ENSP00000488390.2:n.380-24128_380-24127insC
ENST00000492272.6:n.228-24128_228-24127insC
ENST00000642384.2:c.386-24128_386-24127insC MANE Select	ENSP00000496168.1:n.386-24128_386-24127insC
ENST00000642439.1:c.386-30537_386-30536insC	ENSP00000493484.1:n.386-30537_386-30536insC
ENST00000643222.1:c.371-30537_371-30536insC	ENSP00000495862.1:n.371-30537_371-30536insC
ENST00000643459.1:c.371-24128_371-24127insC	ENSP00000494996.1:n.371-24128_371-24127insC
ENST00000644606.1:n.425-24128_425-24127insC
ENST00000645455.1:n.202-24128_202-24127insC
ENST00000646249.1:c.386-30537_386-30536insC	ENSP00000495759.1:n.386-30537_386-30536insC
ENST00000647472.1:c.232-14722_232-14721insC
ENST00000335712.10:c.386-24128_386-24127insC	ENSP00000338774.6:n.386-24128_386-24127insC
ENST00000356842.8:c.386-24128_386-24127insC	ENSP00000349300.4:n.386-24128_386-24127insC
ENST00000358510.5:c.386-30537_386-30536insC	ENSP00000351307.4:n.386-30537_386-30536insC
ENST00000359629.9:c.386-24128_386-24127insC	ENSP00000352648.5:n.386-24128_386-24127insC
ENST00000477659.1:n.69-24128_69-24127insC
ENST00000489516.6:c.230-24128_230-24127insC	ENSP00000488390.1:n.230-24128_230-24127insC
ENST00000492272.5:n.228-24128_228-24127insC
ENST00000631857.1:c.*100+15645_*100+15646insC	ENSP00000488886.1:n.*100+15645_*100+15646insC
NM_018014.3:c.386-24128_386-24127insC	NP_060484.2:n.386-24128_386-24127insC
NM_022893.3:c.386-24128_386-24127insC	NP_075044.2:n.386-24128_386-24127insC
NM_138559.1:c.386-24128_386-24127insC	NP_612569.1:n.386-24128_386-24127insC
XM_011532909.1:c.386-24128_386-24127insC	XP_011531211.1:n.386-24128_386-24127insC
XM_011532910.1:c.386-24128_386-24127insC	XP_011531212.1:n.386-24128_386-24127insC
XM_011532911.1:c.386-30537_386-30536insC	XP_011531213.1:n.386-30537_386-30536insC
XM_011532912.1:c.386-30537_386-30536insC	XP_011531214.1:n.386-30537_386-30536insC
XM_011532913.1:c.380-24128_380-24127insC	XP_011531215.1:n.380-24128_380-24127insC
XM_011532914.1:c.380-30537_380-30536insC	XP_011531216.1:n.380-30537_380-30536insC
XM_011532915.1:c.52+23466_52+23467insC	XP_011531217.1:n.52+23466_52+23467insC
NM_001363864.1:c.386-30537_386-30536insC	NP_001350793.1:n.386-30537_386-30536insC
NM_001365609.1:c.386-30537_386-30536insC	NP_001352538.1:n.386-30537_386-30536insC
XM_017004333.1:c.380-24128_380-24127insC	XP_016859822.1:n.380-24128_380-24127insC
XM_017004335.1:c.380-30537_380-30536insC	XP_016859824.1:n.380-30537_380-30536insC
XM_017004336.1:c.52+23466_52+23467insC	XP_016859825.1:n.52+23466_52+23467insC
XM_024452962.1:c.230-24128_230-24127insC	XP_024308730.1:n.230-24128_230-24127insC
XM_024452963.1:c.230-24128_230-24127insC	XP_024308731.1:n.230-24128_230-24127insC
NM_018014.4:c.386-24128_386-24127insC	NP_060484.2:n.386-24128_386-24127insC
NM_022893.4:c.386-24128_386-24127insC MANE Select	NP_075044.2:n.386-24128_386-24127insC
NM_138559.2:c.386-24128_386-24127insC	NP_612569.1:n.386-24128_386-24127insC