Canonical Allele Identifier: CA2136287641
Gene: ATL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50628319T= , CM000676.2:g.50628319T= GRCh38
NC_000014.8:g.51095037T= , CM000676.1:g.51095037T= GRCh37
NC_000014.7:g.50164787T= NCBI36
NG_009028.1:g.100238T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000553509.2:c.1408T= ENSP00000450989.2:p.Leu470=
ENST00000556478.3:c.1408T= ENSP00000501428.2:p.Leu470=
ENST00000682037.1:c.1408T= ENSP00000508289.1:p.Leu470=
ENST00000682219.1:n.2746T=
ENST00000683037.1:n.1329T=
ENST00000683330.1:n.1742T=
ENST00000358385.12:c.1408T= MANE Select ENSP00000351155.7:p.Leu470=
ENST00000674288.1:c.*2700T= ENSP00000501522.1:n.*2700T=
ENST00000358385.10:c.1408T= ENSP00000351155.6:p.Leu470=
ENST00000441560.6:c.1408T= ENSP00000413675.2:p.Leu470=
ENST00000556067.1:c.154T= ENSP00000451100.1:p.Leu52=
NM_001127713.1:c.1408T= NP_001121185.1:p.Leu470=
NM_015915.4:c.1408T= NP_056999.2:p.Leu470=
NM_181598.3:c.1408T= NP_853629.2:p.Leu470=
NM_015915.5:c.1408T= MANE Select NP_056999.2:p.Leu470=
NM_181598.4:c.1408T= NP_853629.2:p.Leu470=