Canonical Allele Identifier: CA603209626

Gene: AICDA

Linked Data

• dbSNP Id: rs1323219678
• gnomAD v2: 12-8757192-AAAAG-A
• gnomAD v3: 12-8604596-AAAAG-A
• gnomAD v4: 12-8604596-AAAAG-A
• MyVariant Identifiers: chr12:g.8757193_8757196del (hg19) ; chr12:g.8604597_8604600del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604604_8604607del , CM000674.2:g.8604604_8604607del	GRCh38
NC_000012.11:g.8757200_8757203del , CM000674.1:g.8757200_8757203del	GRCh37
NC_000012.10:g.8648467_8648470del	NCBI36
NG_011588.1:g.13247_13250del , LRG_17:g.13247_13250del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.513+207_513+210del	ENSP00000445691.1:n.513+207_513+210del
ENST00000543081.6:c.428-263_428-260del	ENSP00000439103.2:n.428-263_428-260del
ENST00000544516.6:c.157-263_157-260del	ENSP00000439538.2:n.157-263_157-260del
ENST00000545576.2:n.944+207_944+210del
ENST00000696246.1:c.498+207_498+210del	ENSP00000512504.1:n.498+207_498+210del
ENST00000696271.1:n.955+207_955+210del
ENST00000696272.1:c.528+207_528+210del	ENSP00000512515.1:n.528+207_528+210del
ENST00000696273.1:c.576+207_576+210del	ENSP00000512516.1:n.576+207_576+210del
ENST00000229335.11:c.543+207_543+210del MANE Select	ENSP00000229335.6:n.543+207_543+210del
ENST00000229335.10:c.543+207_543+210del	ENSP00000229335.6:n.543+207_543+210del
ENST00000537228.5:c.513+207_513+210del	ENSP00000445691.1:n.513+207_513+210del
ENST00000543081.5:c.424-263_424-260del
ENST00000544516.5:c.153-263_153-260del
ENST00000545512.1:c.539+207_539+210del
ENST00000545576.1:n.869+207_869+210del
NM_020661.2:c.543+207_543+210del , LRG_17t1:c.543+207_543+210del	NP_065712.1:n.543+207_543+210del
XM_011520772.1:c.513+207_513+210del	XP_011519074.1:n.513+207_513+210del
XM_011520773.1:c.428-263_428-260del	XP_011519075.1:n.428-263_428-260del
NM_001330343.1:c.513+207_513+210del	NP_001317272.1:n.513+207_513+210del
NM_020661.3:c.543+207_543+210del	NP_065712.1:n.543+207_543+210del
XM_011520773.2:c.428-263_428-260del	XP_011519075.1:n.428-263_428-260del
NM_020661.4:c.543+207_543+210del MANE Select	NP_065712.1:n.543+207_543+210del
NM_001330343.2:c.513+207_513+210del	NP_001317272.1:n.513+207_513+210del