Canonical Allele Identifier: CA383817921

Gene: AICDA

Linked Data

• gnomAD v3: 12-8604901-G-T
• gnomAD v4: 12-8604901-G-T
• MyVariant Identifiers: chr12:g.8757497G>T (hg19) ; chr12:g.8604901G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604901G>T , CM000674.2:g.8604901G>T	GRCh38
NC_000012.11:g.8757497G>T , CM000674.1:g.8757497G>T	GRCh37
NC_000012.10:g.8648764G>T	NCBI36
NG_011588.1:g.12946C>A , LRG_17:g.12946C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000537228.6:c.428-9C>A	ENSP00000445691.1:n.428-9C>A
ENST00000543081.6:c.427+314C>A	ENSP00000439103.2:n.427+314C>A
ENST00000544516.6:c.157-564C>A	ENSP00000439538.2:n.157-564C>A
ENST00000545576.2:n.850C>A
ENST00000696246.1:c.413-9C>A	ENSP00000512504.1:n.413-9C>A
ENST00000696271.1:n.861C>A
ENST00000696272.1:c.434C>A	ENSP00000512515.1:p.Thr145Asn
ENST00000696273.1:c.482C>A	ENSP00000512516.1:p.Thr161Asn
ENST00000229335.11:c.449C>A MANE Select	ENSP00000229335.6:p.Thr150Asn
ENST00000229335.10:c.449C>A	ENSP00000229335.6:p.Thr150Asn
ENST00000537228.5:c.428-9C>A	ENSP00000445691.1:n.428-9C>A
ENST00000543081.5:c.423+314C>A
ENST00000544516.5:c.153-564C>A
ENST00000545512.1:c.445C>A
ENST00000545576.1:n.775C>A
NM_020661.2:c.449C>A , LRG_17t1:c.449C>A	NP_065712.1:p.Thr150Asn
XM_011520772.1:c.428-9C>A	XP_011519074.1:n.428-9C>A
XM_011520773.1:c.427+314C>A	XP_011519075.1:n.427+314C>A
NM_001330343.1:c.428-9C>A	NP_001317272.1:n.428-9C>A
NM_020661.3:c.449C>A	NP_065712.1:p.Thr150Asn
XM_011520773.2:c.427+314C>A	XP_011519075.1:n.427+314C>A
NM_020661.4:c.449C>A MANE Select	NP_065712.1:p.Thr150Asn
NM_001330343.2:c.428-9C>A	NP_001317272.1:n.428-9C>A