Canonical Allele Identifier: CA2725486165

Gene: AICDA

Linked Data

• dbSNP Id: rs2136431038

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604827_8604849del , CM000674.2:g.8604827_8604849del	GRCh38
NC_000012.11:g.8757423_8757445del , CM000674.1:g.8757423_8757445del	GRCh37
NC_000012.10:g.8648690_8648712del	NCBI36
NG_011588.1:g.12999_13021del , LRG_17:g.12999_13021del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.472_494del	ENSP00000445691.1:p.Asn158AlafsTer10
ENST00000543081.6:c.427+367_427+389del	ENSP00000439103.2:n.427+367_427+389del
ENST00000544516.6:c.157-511_157-489del	ENSP00000439538.2:n.157-511_157-489del
ENST00000545576.2:n.903_925del
ENST00000696246.1:c.457_479del	ENSP00000512504.1:p.Asn153AlafsTer10
ENST00000696271.1:n.914_936del
ENST00000696272.1:c.487_509del	ENSP00000512515.1:p.Asn163AlafsTer10
ENST00000696273.1:c.535_557del	ENSP00000512516.1:p.Asn179AlafsTer10
ENST00000229335.11:c.502_524del MANE Select	ENSP00000229335.6:p.Asn168AlafsTer10
ENST00000229335.10:c.502_524del	ENSP00000229335.6:p.Asn168AlafsTer10
ENST00000537228.5:c.472_494del	ENSP00000445691.1:p.Asn158AlafsTer10
ENST00000543081.5:c.423+367_423+389del
ENST00000544516.5:c.153-511_153-489del
ENST00000545512.1:c.498_520del
ENST00000545576.1:n.828_850del
NM_020661.2:c.502_524del , LRG_17t1:c.502_524del	NP_065712.1:p.Asn168AlafsTer10
XM_011520772.1:c.472_494del	XP_011519074.1:p.Asn158AlafsTer10
XM_011520773.1:c.427+367_427+389del	XP_011519075.1:n.427+367_427+389del
NM_001330343.1:c.472_494del	NP_001317272.1:p.Asn158AlafsTer10
NM_020661.3:c.502_524del	NP_065712.1:p.Asn168AlafsTer10
XM_011520773.2:c.427+367_427+389del	XP_011519075.1:n.427+367_427+389del
NM_020661.4:c.502_524del MANE Select	NP_065712.1:p.Asn168AlafsTer10
NM_001330343.2:c.472_494del	NP_001317272.1:p.Asn158AlafsTer10