Canonical Allele Identifier: CA389671008

Gene: ATL1

Linked Data

• MyVariant Identifiers: chr14:g.51080025T>G (hg19) ; chr14:g.50613307T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50613307T>G , CM000676.2:g.50613307T>G	GRCh38
NC_000014.8:g.51080025T>G , CM000676.1:g.51080025T>G	GRCh37
NC_000014.7:g.50149775T>G	NCBI36
NG_009028.1:g.85226T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000553509.2:c.679T>G	ENSP00000450989.2:p.Tyr227Asp
ENST00000556478.3:c.679T>G	ENSP00000501428.2:p.Tyr227Asp
ENST00000682037.1:c.679T>G	ENSP00000508289.1:p.Tyr227Asp
ENST00000682219.1:n.2017T>G
ENST00000682487.1:n.1013T>G
ENST00000683037.1:n.600T>G
ENST00000683330.1:n.1013T>G
ENST00000683837.1:n.1013T>G
ENST00000358385.12:c.679T>G MANE Select	ENSP00000351155.7:p.Tyr227Asp
ENST00000674288.1:c.*1971T>G	ENSP00000501522.1:n.*1971T>G
ENST00000358385.10:c.679T>G	ENSP00000351155.6:p.Tyr227Asp
ENST00000441560.6:c.679T>G	ENSP00000413675.2:p.Tyr227Asp
NM_001127713.1:c.679T>G	NP_001121185.1:p.Tyr227Asp
NM_015915.4:c.679T>G	NP_056999.2:p.Tyr227Asp
NM_181598.3:c.679T>G	NP_853629.2:p.Tyr227Asp
NM_015915.5:c.679T>G MANE Select	NP_056999.2:p.Tyr227Asp
NM_181598.4:c.679T>G	NP_853629.2:p.Tyr227Asp