Canonical Allele Identifier: CA2136287824
Gene: ATL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50628451C= , CM000676.2:g.50628451C= GRCh38
NC_000014.8:g.51095169C= , CM000676.1:g.51095169C= GRCh37
NC_000014.7:g.50164919C= NCBI36
NG_009028.1:g.100370C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553509.2:c.1540C= ENSP00000450989.2:p.Leu514=
ENST00000556478.3:c.1540C= ENSP00000501428.2:p.Leu514=
ENST00000682037.1:c.1540C= ENSP00000508289.1:p.Leu514=
ENST00000682219.1:n.2878C=
ENST00000683037.1:n.1461C=
ENST00000683330.1:n.1874C=
ENST00000358385.12:c.1540C= MANE Select ENSP00000351155.7:p.Leu514=
ENST00000674288.1:c.*2832C= ENSP00000501522.1:n.*2832C=
ENST00000358385.10:c.1540C= ENSP00000351155.6:p.Leu514=
ENST00000441560.6:c.1540C= ENSP00000413675.2:p.Leu514=
ENST00000556067.1:c.286C= ENSP00000451100.1:p.Leu96=
NM_001127713.1:c.1540C= NP_001121185.1:p.Leu514=
NM_015915.4:c.1540C= NP_056999.2:p.Leu514=
NM_181598.3:c.1540C= NP_853629.2:p.Leu514=
NM_015915.5:c.1540C= MANE Select NP_056999.2:p.Leu514=
NM_181598.4:c.1540C= NP_853629.2:p.Leu514=