Canonical Allele Identifier: CA342181

Gene: ATL1

Linked Data

• ClinVar Variation Id: 21531
• ClinVar RCV Id: RCV000713455 ; RCV000020721
• dbSNP Id: rs137852657
• MyVariant Identifiers: chr14:g.51058302C>T (hg19) ; chr14:g.50591584C>T (hg38)
• PubMed: PMID:20862796

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50591584C>T , CM000676.2:g.50591584C>T	GRCh38
NC_000014.8:g.51058302C>T , CM000676.1:g.51058302C>T	GRCh37
NC_000014.7:g.50128052C>T	NCBI36
NG_009028.1:g.63503C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553509.2:c.467C>T	ENSP00000450989.2:p.Thr156Ile
ENST00000553746.2:n.2425C>T
ENST00000556478.3:c.467C>T	ENSP00000501428.2:p.Thr156Ile
ENST00000682037.1:c.467C>T	ENSP00000508289.1:p.Thr156Ile
ENST00000682219.1:n.1805C>T
ENST00000682226.1:n.801C>T
ENST00000682487.1:n.801C>T
ENST00000683330.1:n.801C>T
ENST00000683703.1:n.801C>T
ENST00000683837.1:n.801C>T
ENST00000684737.1:n.801C>T
ENST00000358385.12:c.467C>T MANE Select	ENSP00000351155.7:p.Thr156Ile
ENST00000674288.1:c.*1759C>T	ENSP00000501522.1:n.*1759C>T
ENST00000674478.1:n.801C>T
ENST00000358385.10:c.467C>T	ENSP00000351155.6:p.Thr156Ile
ENST00000441560.6:c.467C>T	ENSP00000413675.2:p.Thr156Ile
ENST00000553746.1:n.137C>T
ENST00000554886.1:c.35C>T	ENSP00000452074.1:p.Thr12Ile
NM_001127713.1:c.467C>T	NP_001121185.1:p.Thr156Ile
NM_015915.4:c.467C>T	NP_056999.2:p.Thr156Ile
NM_181598.3:c.467C>T	NP_853629.2:p.Thr156Ile
NM_015915.5:c.467C>T MANE Select	NP_056999.2:p.Thr156Ile
NM_181598.4:c.467C>T	NP_853629.2:p.Thr156Ile