Canonical Allele Identifier: CA383817703

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8757464G>T (hg19) ; chr12:g.8604868G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604868G>T , CM000674.2:g.8604868G>T	GRCh38
NC_000012.11:g.8757464G>T , CM000674.1:g.8757464G>T	GRCh37
NC_000012.10:g.8648731G>T	NCBI36
NG_011588.1:g.12979C>A , LRG_17:g.12979C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.452C>A	ENSP00000445691.1:p.Ala151Asp
ENST00000543081.6:c.427+347C>A	ENSP00000439103.2:n.427+347C>A
ENST00000544516.6:c.157-531C>A	ENSP00000439538.2:n.157-531C>A
ENST00000545576.2:n.883C>A
ENST00000696246.1:c.437C>A	ENSP00000512504.1:p.Ala146Asp
ENST00000696271.1:n.894C>A
ENST00000696272.1:c.467C>A	ENSP00000512515.1:p.Ala156Asp
ENST00000696273.1:c.515C>A	ENSP00000512516.1:p.Ala172Asp
ENST00000229335.11:c.482C>A MANE Select	ENSP00000229335.6:p.Ala161Asp
ENST00000229335.10:c.482C>A	ENSP00000229335.6:p.Ala161Asp
ENST00000537228.5:c.452C>A	ENSP00000445691.1:p.Ala151Asp
ENST00000543081.5:c.423+347C>A
ENST00000544516.5:c.153-531C>A
ENST00000545512.1:c.478C>A
ENST00000545576.1:n.808C>A
NM_020661.2:c.482C>A , LRG_17t1:c.482C>A	NP_065712.1:p.Ala161Asp
XM_011520772.1:c.452C>A	XP_011519074.1:p.Ala151Asp
XM_011520773.1:c.427+347C>A	XP_011519075.1:n.427+347C>A
NM_001330343.1:c.452C>A	NP_001317272.1:p.Ala151Asp
NM_020661.3:c.482C>A	NP_065712.1:p.Ala161Asp
XM_011520773.2:c.427+347C>A	XP_011519075.1:n.427+347C>A
NM_020661.4:c.482C>A MANE Select	NP_065712.1:p.Ala161Asp
NM_001330343.2:c.452C>A	NP_001317272.1:p.Ala151Asp