Canonical Allele Identifier: CA2015109340

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604496_8604514delinsTAAAAAAAAAAAAAAAAAA , CM000674.2:g.8604496_8604514delinsTAAAAAAAAAAAAAAAAAA	GRCh38
NC_000012.11:g.8757092_8757110delinsTAAAAAAAAAAAAAAAAAA , CM000674.1:g.8757092_8757110delinsTAAAAAAAAAAAAAAAAAA	GRCh37
NC_000012.10:g.8648359_8648377delinsTAAAAAAAAAAAAAAAAAA	NCBI36
NG_011588.1:g.13333_13351delinsTTTTTTTTTTTTTTTTTTA , LRG_17:g.13333_13351delinsTTTTTTTTTTTTTTTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.514-177_514-159delinsTTTTTTTTTTTTTTTTTTA	ENSP00000445691.1:n.514-177_514-159delinsTTTTTTTTTTTTTTTTTTA
ENST00000543081.6:c.428-177_428-159delinsTTTTTTTTTTTTTTTTTTA	ENSP00000439103.2:n.428-177_428-159delinsTTTTTTTTTTTTTTTTTTA
ENST00000544516.6:c.157-177_157-159delinsTTTTTTTTTTTTTTTTTTA	ENSP00000439538.2:n.157-177_157-159delinsTTTTTTTTTTTTTTTTTTA
ENST00000545576.2:n.945-177_945-159delinsTTTTTTTTTTTTTTTTTTA
ENST00000696246.1:c.499-177_499-159delinsTTTTTTTTTTTTTTTTTTA	ENSP00000512504.1:n.499-177_499-159delinsTTTTTTTTTTTTTTTTTTA
ENST00000696271.1:n.956-177_956-159delinsTTTTTTTTTTTTTTTTTTA
ENST00000696272.1:c.529-177_529-159delinsTTTTTTTTTTTTTTTTTTA	ENSP00000512515.1:n.529-177_529-159delinsTTTTTTTTTTTTTTTTTTA
ENST00000696273.1:c.577-177_577-159delinsTTTTTTTTTTTTTTTTTTA	ENSP00000512516.1:n.577-177_577-159delinsTTTTTTTTTTTTTTTTTTA
ENST00000229335.11:c.544-177_544-159delinsTTTTTTTTTTTTTTTTTTA MANE Select	ENSP00000229335.6:n.544-177_544-159delinsTTTTTTTTTTTTTTTTTTA
ENST00000229335.10:c.544-177_544-159delinsTTTTTTTTTTTTTTTTTTA	ENSP00000229335.6:n.544-177_544-159delinsTTTTTTTTTTTTTTTTTTA
ENST00000537228.5:c.514-177_514-159delinsTTTTTTTTTTTTTTTTTTA	ENSP00000445691.1:n.514-177_514-159delinsTTTTTTTTTTTTTTTTTTA
ENST00000543081.5:c.424-177_424-159delinsTTTTTTTTTTTTTTTTTTA
ENST00000544516.5:c.153-177_153-159delinsTTTTTTTTTTTTTTTTTTA
ENST00000545512.1:c.540-177_540-159delinsTTTTTTTTTTTTTTTTTTA
ENST00000545576.1:n.870-177_870-159delinsTTTTTTTTTTTTTTTTTTA
NM_020661.2:c.544-177_544-159delinsTTTTTTTTTTTTTTTTTTA , LRG_17t1:c.544-177_544-159delinsTTTTTTTTTTTTTTTTTTA	NP_065712.1:n.544-177_544-159delinsTTTTTTTTTTTTTTTTTTA
XM_011520772.1:c.514-177_514-159delinsTTTTTTTTTTTTTTTTTTA	XP_011519074.1:n.514-177_514-159delinsTTTTTTTTTTTTTTTTTTA
XM_011520773.1:c.428-177_428-159delinsTTTTTTTTTTTTTTTTTTA	XP_011519075.1:n.428-177_428-159delinsTTTTTTTTTTTTTTTTTTA
NM_001330343.1:c.514-177_514-159delinsTTTTTTTTTTTTTTTTTTA	NP_001317272.1:n.514-177_514-159delinsTTTTTTTTTTTTTTTTTTA
NM_020661.3:c.544-177_544-159delinsTTTTTTTTTTTTTTTTTTA	NP_065712.1:n.544-177_544-159delinsTTTTTTTTTTTTTTTTTTA
XM_011520773.2:c.428-177_428-159delinsTTTTTTTTTTTTTTTTTTA	XP_011519075.1:n.428-177_428-159delinsTTTTTTTTTTTTTTTTTTA
NM_020661.4:c.544-177_544-159delinsTTTTTTTTTTTTTTTTTTA MANE Select	NP_065712.1:n.544-177_544-159delinsTTTTTTTTTTTTTTTTTTA
NM_001330343.2:c.514-177_514-159delinsTTTTTTTTTTTTTTTTTTA	NP_001317272.1:n.514-177_514-159delinsTTTTTTTTTTTTTTTTTTA