Canonical Allele Identifier: CA2015109802

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604909G= , CM000674.2:g.8604909G=	GRCh38
NC_000012.11:g.8757505G= , CM000674.1:g.8757505G=	GRCh37
NC_000012.10:g.8648772G=	NCBI36
NG_011588.1:g.12938C= , LRG_17:g.12938C=

Transcript Alleles

HGVS	Amino-acid Change
NM_020661.4:c.441C= MANE Select	NP_065712.1:p.Cys147=
ENST00000229335.11:c.441C= MANE Select	ENSP00000229335.6:p.Cys147=
NM_001330343.1:c.428-17C=	NP_001317272.1:n.428-17C=
NM_001330343.2:c.428-17C=	NP_001317272.1:n.428-17C=
NM_020661.2:c.441C= , LRG_17t1:c.441C=	NP_065712.1:p.Cys147=
NM_020661.3:c.441C=	NP_065712.1:p.Cys147=
ENST00000229335.10:c.441C=	ENSP00000229335.6:p.Cys147=
ENST00000537228.5:c.428-17C=	ENSP00000445691.1:n.428-17C=
ENST00000537228.6:c.428-17C=	ENSP00000445691.1:n.428-17C=
ENST00000543081.5:c.423+306C=
ENST00000543081.6:c.427+306C=	ENSP00000439103.2:n.427+306C=
ENST00000544516.5:c.153-572C=
ENST00000544516.6:c.157-572C=	ENSP00000439538.2:n.157-572C=
ENST00000545512.1:c.437C=
ENST00000545576.1:n.767C=
ENST00000545576.2:n.842C=
ENST00000696246.1:c.413-17C=	ENSP00000512504.1:n.413-17C=
ENST00000696271.1:n.853C=
ENST00000696272.1:c.426C=	ENSP00000512515.1:p.Cys142=
ENST00000696273.1:c.474C=	ENSP00000512516.1:p.Cys158=
XM_011520772.1:c.428-17C=	XP_011519074.1:n.428-17C=
XM_011520773.1:c.427+306C=	XP_011519075.1:n.427+306C=
XM_011520773.2:c.427+306C=	XP_011519075.1:n.427+306C=