Canonical Allele Identifier: CA383817681

Gene: AICDA

Linked Data

• MyVariant Identifiers: chr12:g.8757460C>T (hg19) ; chr12:g.8604864C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.8604864C>T , CM000674.2:g.8604864C>T	GRCh38
NC_000012.11:g.8757460C>T , CM000674.1:g.8757460C>T	GRCh37
NC_000012.10:g.8648727C>T	NCBI36
NG_011588.1:g.12983G>A , LRG_17:g.12983G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000537228.6:c.456G>A	ENSP00000445691.1:p.Trp152Ter
ENST00000543081.6:c.427+351G>A	ENSP00000439103.2:n.427+351G>A
ENST00000544516.6:c.157-527G>A	ENSP00000439538.2:n.157-527G>A
ENST00000545576.2:n.887G>A
ENST00000696246.1:c.441G>A	ENSP00000512504.1:p.Trp147Ter
ENST00000696271.1:n.898G>A
ENST00000696272.1:c.471G>A	ENSP00000512515.1:p.Trp157Ter
ENST00000696273.1:c.519G>A	ENSP00000512516.1:p.Trp173Ter
ENST00000229335.11:c.486G>A MANE Select	ENSP00000229335.6:p.Trp162Ter
ENST00000229335.10:c.486G>A	ENSP00000229335.6:p.Trp162Ter
ENST00000537228.5:c.456G>A	ENSP00000445691.1:p.Trp152Ter
ENST00000543081.5:c.423+351G>A
ENST00000544516.5:c.153-527G>A
ENST00000545512.1:c.482G>A
ENST00000545576.1:n.812G>A
NM_020661.2:c.486G>A , LRG_17t1:c.486G>A	NP_065712.1:p.Trp162Ter
XM_011520772.1:c.456G>A	XP_011519074.1:p.Trp152Ter
XM_011520773.1:c.427+351G>A	XP_011519075.1:n.427+351G>A
NM_001330343.1:c.456G>A	NP_001317272.1:p.Trp152Ter
NM_020661.3:c.486G>A	NP_065712.1:p.Trp162Ter
XM_011520773.2:c.427+351G>A	XP_011519075.1:n.427+351G>A
NM_020661.4:c.486G>A MANE Select	NP_065712.1:p.Trp162Ter
NM_001330343.2:c.456G>A	NP_001317272.1:p.Trp152Ter