Canonical Allele Identifier: CA383817936

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8757500T>A (hg19) ; chr12:g.8604904T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604904T>A , CM000674.2:g.8604904T>A	GRCh38
NC_000012.11:g.8757500T>A , CM000674.1:g.8757500T>A	GRCh37
NC_000012.10:g.8648767T>A	NCBI36
NG_011588.1:g.12943A>T , LRG_17:g.12943A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000537228.6:c.428-12A>T	ENSP00000445691.1:n.428-12A>T
ENST00000543081.6:c.427+311A>T	ENSP00000439103.2:n.427+311A>T
ENST00000544516.6:c.157-567A>T	ENSP00000439538.2:n.157-567A>T
ENST00000545576.2:n.847A>T
ENST00000696246.1:c.413-12A>T	ENSP00000512504.1:n.413-12A>T
ENST00000696271.1:n.858A>T
ENST00000696272.1:c.431A>T	ENSP00000512515.1:p.Asn144Ile
ENST00000696273.1:c.479A>T	ENSP00000512516.1:p.Asn160Ile
ENST00000229335.11:c.446A>T MANE Select	ENSP00000229335.6:p.Asn149Ile
ENST00000229335.10:c.446A>T	ENSP00000229335.6:p.Asn149Ile
ENST00000537228.5:c.428-12A>T	ENSP00000445691.1:n.428-12A>T
ENST00000543081.5:c.423+311A>T
ENST00000544516.5:c.153-567A>T
ENST00000545512.1:c.442A>T
ENST00000545576.1:n.772A>T
NM_020661.2:c.446A>T , LRG_17t1:c.446A>T	NP_065712.1:p.Asn149Ile
XM_011520772.1:c.428-12A>T	XP_011519074.1:n.428-12A>T
XM_011520773.1:c.427+311A>T	XP_011519075.1:n.427+311A>T
NM_001330343.1:c.428-12A>T	NP_001317272.1:n.428-12A>T
NM_020661.3:c.446A>T	NP_065712.1:p.Asn149Ile
XM_011520773.2:c.427+311A>T	XP_011519075.1:n.427+311A>T
NM_020661.4:c.446A>T MANE Select	NP_065712.1:p.Asn149Ile
NM_001330343.2:c.428-12A>T	NP_001317272.1:n.428-12A>T