Canonical Allele Identifier: CA2015109428

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604519_8604524delinsAAAAAG , CM000674.2:g.8604519_8604524delinsAAAAAG	GRCh38
NC_000012.11:g.8757115_8757120delinsAAAAAG , CM000674.1:g.8757115_8757120delinsAAAAAG	GRCh37
NC_000012.10:g.8648382_8648387delinsAAAAAG	NCBI36
NG_011588.1:g.13323_13328delinsCTTTTT , LRG_17:g.13323_13328delinsCTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.514-187_514-182delinsCTTTTT	ENSP00000445691.1:n.514-187_514-182delinsCTTTTT
ENST00000543081.6:c.428-187_428-182delinsCTTTTT	ENSP00000439103.2:n.428-187_428-182delinsCTTTTT
ENST00000544516.6:c.157-187_157-182delinsCTTTTT	ENSP00000439538.2:n.157-187_157-182delinsCTTTTT
ENST00000545576.2:n.945-187_945-182delinsCTTTTT
ENST00000696246.1:c.499-187_499-182delinsCTTTTT	ENSP00000512504.1:n.499-187_499-182delinsCTTTTT
ENST00000696271.1:n.956-187_956-182delinsCTTTTT
ENST00000696272.1:c.529-187_529-182delinsCTTTTT	ENSP00000512515.1:n.529-187_529-182delinsCTTTTT
ENST00000696273.1:c.577-187_577-182delinsCTTTTT	ENSP00000512516.1:n.577-187_577-182delinsCTTTTT
ENST00000229335.11:c.544-187_544-182delinsCTTTTT MANE Select	ENSP00000229335.6:n.544-187_544-182delinsCTTTTT
ENST00000229335.10:c.544-187_544-182delinsCTTTTT	ENSP00000229335.6:n.544-187_544-182delinsCTTTTT
ENST00000537228.5:c.514-187_514-182delinsCTTTTT	ENSP00000445691.1:n.514-187_514-182delinsCTTTTT
ENST00000543081.5:c.424-187_424-182delinsCTTTTT
ENST00000544516.5:c.153-187_153-182delinsCTTTTT
ENST00000545512.1:c.540-187_540-182delinsCTTTTT
ENST00000545576.1:n.870-187_870-182delinsCTTTTT
NM_020661.2:c.544-187_544-182delinsCTTTTT , LRG_17t1:c.544-187_544-182delinsCTTTTT	NP_065712.1:n.544-187_544-182delinsCTTTTT
XM_011520772.1:c.514-187_514-182delinsCTTTTT	XP_011519074.1:n.514-187_514-182delinsCTTTTT
XM_011520773.1:c.428-187_428-182delinsCTTTTT	XP_011519075.1:n.428-187_428-182delinsCTTTTT
NM_001330343.1:c.514-187_514-182delinsCTTTTT	NP_001317272.1:n.514-187_514-182delinsCTTTTT
NM_020661.3:c.544-187_544-182delinsCTTTTT	NP_065712.1:n.544-187_544-182delinsCTTTTT
XM_011520773.2:c.428-187_428-182delinsCTTTTT	XP_011519075.1:n.428-187_428-182delinsCTTTTT
NM_020661.4:c.544-187_544-182delinsCTTTTT MANE Select	NP_065712.1:n.544-187_544-182delinsCTTTTT
NM_001330343.2:c.514-187_514-182delinsCTTTTT	NP_001317272.1:n.514-187_514-182delinsCTTTTT