Canonical Allele Identifier: CA2617496369

Gene: AICDA

Linked Data

• gnomAD v4: 12-8604707-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604711_8604712del , CM000674.2:g.8604711_8604712del	GRCh38
NC_000012.11:g.8757307_8757308del , CM000674.1:g.8757307_8757308del	GRCh37
NC_000012.10:g.8648574_8648575del	NCBI36
NG_011588.1:g.13138_13139del , LRG_17:g.13138_13139del

Transcript Alleles

HGVS	Amino-acid change
ENST00000537228.6:c.513+98_513+99del	ENSP00000445691.1:n.513+98_513+99del
ENST00000543081.6:c.428-372_428-371del	ENSP00000439103.2:n.428-372_428-371del
ENST00000544516.6:c.157-372_157-371del	ENSP00000439538.2:n.157-372_157-371del
ENST00000545576.2:n.944+98_944+99del
ENST00000696246.1:c.498+98_498+99del	ENSP00000512504.1:n.498+98_498+99del
ENST00000696271.1:n.955+98_955+99del
ENST00000696272.1:c.528+98_528+99del	ENSP00000512515.1:n.528+98_528+99del
ENST00000696273.1:c.576+98_576+99del	ENSP00000512516.1:n.576+98_576+99del
ENST00000229335.11:c.543+98_543+99del MANE Select	ENSP00000229335.6:n.543+98_543+99del
ENST00000229335.10:c.543+98_543+99del	ENSP00000229335.6:n.543+98_543+99del
ENST00000537228.5:c.513+98_513+99del	ENSP00000445691.1:n.513+98_513+99del
ENST00000543081.5:c.424-372_424-371del
ENST00000544516.5:c.153-372_153-371del
ENST00000545512.1:c.539+98_539+99del
ENST00000545576.1:n.869+98_869+99del
NM_020661.2:c.543+98_543+99del , LRG_17t1:c.543+98_543+99del	NP_065712.1:n.543+98_543+99del
XM_011520772.1:c.513+98_513+99del	XP_011519074.1:n.513+98_513+99del
XM_011520773.1:c.428-372_428-371del	XP_011519075.1:n.428-372_428-371del
NM_001330343.1:c.513+98_513+99del	NP_001317272.1:n.513+98_513+99del
NM_020661.3:c.543+98_543+99del	NP_065712.1:n.543+98_543+99del
XM_011520773.2:c.428-372_428-371del	XP_011519075.1:n.428-372_428-371del
NM_020661.4:c.543+98_543+99del MANE Select	NP_065712.1:n.543+98_543+99del
NM_001330343.2:c.513+98_513+99del	NP_001317272.1:n.513+98_513+99del