Canonical Allele Identifier: CA2136274968
Gene: ATL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50613306A= , CM000676.2:g.50613306A= GRCh38
NC_000014.8:g.51080024A= , CM000676.1:g.51080024A= GRCh37
NC_000014.7:g.50149774A= NCBI36
NG_009028.1:g.85225A=

Transcript Alleles

HGVS Amino-acid change
ENST00000553509.2:c.678A= ENSP00000450989.2:p.Ser226=
ENST00000556478.3:c.678A= ENSP00000501428.2:p.Ser226=
ENST00000682037.1:c.678A= ENSP00000508289.1:p.Ser226=
ENST00000682219.1:n.2016A=
ENST00000682487.1:n.1012A=
ENST00000683037.1:n.599A=
ENST00000683330.1:n.1012A=
ENST00000683837.1:n.1012A=
ENST00000358385.12:c.678A= MANE Select ENSP00000351155.7:p.Ser226=
ENST00000674288.1:c.*1970A= ENSP00000501522.1:n.*1970A=
ENST00000358385.10:c.678A= ENSP00000351155.6:p.Ser226=
ENST00000441560.6:c.678A= ENSP00000413675.2:p.Ser226=
NM_001127713.1:c.678A= NP_001121185.1:p.Ser226=
NM_015915.4:c.678A= NP_056999.2:p.Ser226=
NM_181598.3:c.678A= NP_853629.2:p.Ser226=
NM_015915.5:c.678A= MANE Select NP_056999.2:p.Ser226=
NM_181598.4:c.678A= NP_853629.2:p.Ser226=