Canonical Allele Identifier: CA2617496355

Gene: AICDA

Linked Data

• gnomAD v4: 12-8604684-TAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604686_8604687del , CM000674.2:g.8604686_8604687del	GRCh38
NC_000012.11:g.8757282_8757283del , CM000674.1:g.8757282_8757283del	GRCh37
NC_000012.10:g.8648549_8648550del	NCBI36
NG_011588.1:g.13161_13162del , LRG_17:g.13161_13162del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.513+121_513+122del	ENSP00000445691.1:n.513+121_513+122del
ENST00000543081.6:c.428-349_428-348del	ENSP00000439103.2:n.428-349_428-348del
ENST00000544516.6:c.157-349_157-348del	ENSP00000439538.2:n.157-349_157-348del
ENST00000545576.2:n.944+121_944+122del
ENST00000696246.1:c.498+121_498+122del	ENSP00000512504.1:n.498+121_498+122del
ENST00000696271.1:n.955+121_955+122del
ENST00000696272.1:c.528+121_528+122del	ENSP00000512515.1:n.528+121_528+122del
ENST00000696273.1:c.576+121_576+122del	ENSP00000512516.1:n.576+121_576+122del
ENST00000229335.11:c.543+121_543+122del MANE Select	ENSP00000229335.6:n.543+121_543+122del
ENST00000229335.10:c.543+121_543+122del	ENSP00000229335.6:n.543+121_543+122del
ENST00000537228.5:c.513+121_513+122del	ENSP00000445691.1:n.513+121_513+122del
ENST00000543081.5:c.424-349_424-348del
ENST00000544516.5:c.153-349_153-348del
ENST00000545512.1:c.539+121_539+122del
ENST00000545576.1:n.869+121_869+122del
NM_020661.2:c.543+121_543+122del , LRG_17t1:c.543+121_543+122del	NP_065712.1:n.543+121_543+122del
XM_011520772.1:c.513+121_513+122del	XP_011519074.1:n.513+121_513+122del
XM_011520773.1:c.428-349_428-348del	XP_011519075.1:n.428-349_428-348del
NM_001330343.1:c.513+121_513+122del	NP_001317272.1:n.513+121_513+122del
NM_020661.3:c.543+121_543+122del	NP_065712.1:n.543+121_543+122del
XM_011520773.2:c.428-349_428-348del	XP_011519075.1:n.428-349_428-348del
NM_020661.4:c.543+121_543+122del MANE Select	NP_065712.1:n.543+121_543+122del
NM_001330343.2:c.513+121_513+122del	NP_001317272.1:n.513+121_513+122del