Canonical Allele Identifier: CA2015109695
Gene: AICDA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.8604801C= , CM000674.2:g.8604801C= GRCh38
NC_000012.11:g.8757397C= , CM000674.1:g.8757397C= GRCh37
NC_000012.10:g.8648664C= NCBI36
NG_011588.1:g.13046G= , LRG_17:g.13046G=

Transcript Alleles

HGVS Amino-acid change
ENST00000537228.6:c.513+6G= ENSP00000445691.1:n.513+6G=
ENST00000543081.6:c.427+414G= ENSP00000439103.2:n.427+414G=
ENST00000544516.6:c.157-464G= ENSP00000439538.2:n.157-464G=
ENST00000545576.2:n.944+6G=
ENST00000696246.1:c.498+6G= ENSP00000512504.1:n.498+6G=
ENST00000696271.1:n.955+6G=
ENST00000696272.1:c.528+6G= ENSP00000512515.1:n.528+6G=
ENST00000696273.1:c.576+6G= ENSP00000512516.1:n.576+6G=
ENST00000229335.11:c.543+6G= MANE Select ENSP00000229335.6:n.543+6G=
ENST00000229335.10:c.543+6G= ENSP00000229335.6:n.543+6G=
ENST00000537228.5:c.513+6G= ENSP00000445691.1:n.513+6G=
ENST00000543081.5:c.423+414G=
ENST00000544516.5:c.153-464G=
ENST00000545512.1:c.539+6G=
ENST00000545576.1:n.869+6G=
NM_020661.2:c.543+6G= , LRG_17t1:c.543+6G= NP_065712.1:n.543+6G=
XM_011520772.1:c.513+6G= XP_011519074.1:n.513+6G=
XM_011520773.1:c.427+414G= XP_011519075.1:n.427+414G=
NM_001330343.1:c.513+6G= NP_001317272.1:n.513+6G=
NM_020661.3:c.543+6G= NP_065712.1:n.543+6G=
XM_011520773.2:c.427+414G= XP_011519075.1:n.427+414G=
NM_020661.4:c.543+6G= MANE Select NP_065712.1:n.543+6G=
NM_001330343.2:c.513+6G= NP_001317272.1:n.513+6G=