Canonical Allele Identifier: CA2015109523

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604596_8604600delinsAAAAG , CM000674.2:g.8604596_8604600delinsAAAAG	GRCh38
NC_000012.11:g.8757192_8757196delinsAAAAG , CM000674.1:g.8757192_8757196delinsAAAAG	GRCh37
NC_000012.10:g.8648459_8648463delinsAAAAG	NCBI36
NG_011588.1:g.13247_13251delinsCTTTT , LRG_17:g.13247_13251delinsCTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.513+207_513+211delinsCTTTT	ENSP00000445691.1:n.513+207_513+211delinsCTTTT
ENST00000543081.6:c.428-263_428-259delinsCTTTT	ENSP00000439103.2:n.428-263_428-259delinsCTTTT
ENST00000544516.6:c.157-263_157-259delinsCTTTT	ENSP00000439538.2:n.157-263_157-259delinsCTTTT
ENST00000545576.2:n.944+207_944+211delinsCTTTT
ENST00000696246.1:c.498+207_498+211delinsCTTTT	ENSP00000512504.1:n.498+207_498+211delinsCTTTT
ENST00000696271.1:n.955+207_955+211delinsCTTTT
ENST00000696272.1:c.528+207_528+211delinsCTTTT	ENSP00000512515.1:n.528+207_528+211delinsCTTTT
ENST00000696273.1:c.576+207_576+211delinsCTTTT	ENSP00000512516.1:n.576+207_576+211delinsCTTTT
ENST00000229335.11:c.543+207_543+211delinsCTTTT MANE Select	ENSP00000229335.6:n.543+207_543+211delinsCTTTT
ENST00000229335.10:c.543+207_543+211delinsCTTTT	ENSP00000229335.6:n.543+207_543+211delinsCTTTT
ENST00000537228.5:c.513+207_513+211delinsCTTTT	ENSP00000445691.1:n.513+207_513+211delinsCTTTT
ENST00000543081.5:c.424-263_424-259delinsCTTTT
ENST00000544516.5:c.153-263_153-259delinsCTTTT
ENST00000545512.1:c.539+207_539+211delinsCTTTT
ENST00000545576.1:n.869+207_869+211delinsCTTTT
NM_020661.2:c.543+207_543+211delinsCTTTT , LRG_17t1:c.543+207_543+211delinsCTTTT	NP_065712.1:n.543+207_543+211delinsCTTTT
XM_011520772.1:c.513+207_513+211delinsCTTTT	XP_011519074.1:n.513+207_513+211delinsCTTTT
XM_011520773.1:c.428-263_428-259delinsCTTTT	XP_011519075.1:n.428-263_428-259delinsCTTTT
NM_001330343.1:c.513+207_513+211delinsCTTTT	NP_001317272.1:n.513+207_513+211delinsCTTTT
NM_020661.3:c.543+207_543+211delinsCTTTT	NP_065712.1:n.543+207_543+211delinsCTTTT
XM_011520773.2:c.428-263_428-259delinsCTTTT	XP_011519075.1:n.428-263_428-259delinsCTTTT
NM_020661.4:c.543+207_543+211delinsCTTTT MANE Select	NP_065712.1:n.543+207_543+211delinsCTTTT
NM_001330343.2:c.513+207_513+211delinsCTTTT	NP_001317272.1:n.513+207_513+211delinsCTTTT