Canonical Allele Identifier: CA486191399
Gene: ATL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50614430_50614431insA , CM000676.2:g.50614430_50614431insA GRCh38
NC_000014.8:g.51081148_51081149insA , CM000676.1:g.51081148_51081149insA GRCh37
NC_000014.7:g.50150898_50150899insA NCBI36
NG_009028.1:g.86349_86350insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000553509.2:c.781_782insA ENSP00000450989.2:p.Phe261TyrfsTer23
ENST00000556478.3:c.781_782insA ENSP00000501428.2:p.Phe261TyrfsTer23
ENST00000682037.1:c.781_782insA ENSP00000508289.1:p.Phe261TyrfsTer23
ENST00000682219.1:n.2119_2120insA
ENST00000682487.1:n.1115_1116insA
ENST00000683037.1:n.702_703insA
ENST00000683330.1:n.1115_1116insA
ENST00000683837.1:n.1115_1116insA
ENST00000358385.12:c.781_782insA MANE Select ENSP00000351155.7:p.Phe261TyrfsTer23
ENST00000674288.1:c.*2073_*2074insA ENSP00000501522.1:n.*2073_*2074insA
ENST00000358385.10:c.781_782insA ENSP00000351155.6:p.Phe261TyrfsTer23
ENST00000441560.6:c.781_782insA ENSP00000413675.2:p.Phe261TyrfsTer23
ENST00000555266.1:c.52_53insA ENSP00000450897.1:p.Phe18TyrfsTer23
NM_001127713.1:c.781_782insA NP_001121185.1:p.Phe261TyrfsTer23
NM_015915.4:c.781_782insA NP_056999.2:p.Phe261TyrfsTer23
NM_181598.3:c.781_782insA NP_853629.2:p.Phe261TyrfsTer23
NM_015915.5:c.781_782insA MANE Select NP_056999.2:p.Phe261TyrfsTer23
NM_181598.4:c.781_782insA NP_853629.2:p.Phe261TyrfsTer23