Canonical Allele Identifier: CA2015109528

Gene: AICDA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604600_8604605delinsGAAAGA , CM000674.2:g.8604600_8604605delinsGAAAGA	GRCh38
NC_000012.11:g.8757196_8757201delinsGAAAGA , CM000674.1:g.8757196_8757201delinsGAAAGA	GRCh37
NC_000012.10:g.8648463_8648468delinsGAAAGA	NCBI36
NG_011588.1:g.13242_13247delinsTCTTTC , LRG_17:g.13242_13247delinsTCTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.513+202_513+207delinsTCTTTC	ENSP00000445691.1:n.513+202_513+207delinsTCTTTC
ENST00000543081.6:c.428-268_428-263delinsTCTTTC	ENSP00000439103.2:n.428-268_428-263delinsTCTTTC
ENST00000544516.6:c.157-268_157-263delinsTCTTTC	ENSP00000439538.2:n.157-268_157-263delinsTCTTTC
ENST00000545576.2:n.944+202_944+207delinsTCTTTC
ENST00000696246.1:c.498+202_498+207delinsTCTTTC	ENSP00000512504.1:n.498+202_498+207delinsTCTTTC
ENST00000696271.1:n.955+202_955+207delinsTCTTTC
ENST00000696272.1:c.528+202_528+207delinsTCTTTC	ENSP00000512515.1:n.528+202_528+207delinsTCTTTC
ENST00000696273.1:c.576+202_576+207delinsTCTTTC	ENSP00000512516.1:n.576+202_576+207delinsTCTTTC
ENST00000229335.11:c.543+202_543+207delinsTCTTTC MANE Select	ENSP00000229335.6:n.543+202_543+207delinsTCTTTC
ENST00000229335.10:c.543+202_543+207delinsTCTTTC	ENSP00000229335.6:n.543+202_543+207delinsTCTTTC
ENST00000537228.5:c.513+202_513+207delinsTCTTTC	ENSP00000445691.1:n.513+202_513+207delinsTCTTTC
ENST00000543081.5:c.424-268_424-263delinsTCTTTC
ENST00000544516.5:c.153-268_153-263delinsTCTTTC
ENST00000545512.1:c.539+202_539+207delinsTCTTTC
ENST00000545576.1:n.869+202_869+207delinsTCTTTC
NM_020661.2:c.543+202_543+207delinsTCTTTC , LRG_17t1:c.543+202_543+207delinsTCTTTC	NP_065712.1:n.543+202_543+207delinsTCTTTC
XM_011520772.1:c.513+202_513+207delinsTCTTTC	XP_011519074.1:n.513+202_513+207delinsTCTTTC
XM_011520773.1:c.428-268_428-263delinsTCTTTC	XP_011519075.1:n.428-268_428-263delinsTCTTTC
NM_001330343.1:c.513+202_513+207delinsTCTTTC	NP_001317272.1:n.513+202_513+207delinsTCTTTC
NM_020661.3:c.543+202_543+207delinsTCTTTC	NP_065712.1:n.543+202_543+207delinsTCTTTC
XM_011520773.2:c.428-268_428-263delinsTCTTTC	XP_011519075.1:n.428-268_428-263delinsTCTTTC
NM_020661.4:c.543+202_543+207delinsTCTTTC MANE Select	NP_065712.1:n.543+202_543+207delinsTCTTTC
NM_001330343.2:c.513+202_513+207delinsTCTTTC	NP_001317272.1:n.513+202_513+207delinsTCTTTC