Canonical Allele Identifier: CA2158268431

Gene: BCL11B

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.99175513A= , CM000676.2:g.99175513A=	GRCh38
NC_000014.8:g.99641850A= , CM000676.1:g.99641850A=	GRCh37
NC_000014.7:g.98711603A=	NCBI36
NG_027894.1:g.100973T=

Transcript Alleles

HGVS	Amino-acid Change
NM_138576.4:c.1323T= MANE Select	NP_612808.1:p.Asn441=
ENST00000357195.8:c.1323T= MANE Select	ENSP00000349723.3:p.Asn441=
NM_001282237.1:c.1320T=	NP_001269166.1:p.Asn440=
NM_001282237.2:c.1320T=	NP_001269166.1:p.Asn440=
NM_001282238.1:c.1107T=	NP_001269167.1:p.Asn369=
NM_001282238.2:c.1107T=	NP_001269167.1:p.Asn369=
NM_022898.2:c.1110T=	NP_075049.1:p.Asn370=
NM_022898.3:c.1110T=	NP_075049.1:p.Asn370=
NM_138576.3:c.1323T=	NP_612808.1:p.Asn441=
ENST00000345514.2:c.1110T=	ENSP00000280435.6:p.Asn370=
ENST00000357195.7:c.1323T=	ENSP00000349723.3:p.Asn441=
ENST00000443726.2:c.741T=	ENSP00000387419.2:p.Asn247=
XM_011537100.1:c.1185T=	XP_011535402.1:p.Asn395=