Canonical Allele Identifier: CA2136253248
Gene: ATL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.50587881G= , CM000676.2:g.50587881G= GRCh38
NC_000014.8:g.51054599G= , CM000676.1:g.51054599G= GRCh37
NC_000014.7:g.50124349G= NCBI36
NG_009028.1:g.59800G=

Transcript Alleles

HGVS Amino-acid change
ENST00000553509.2:c.85G= ENSP00000450989.2:p.Val29=
ENST00000553746.2:n.286G=
ENST00000556478.3:c.85G= ENSP00000501428.2:p.Val29=
ENST00000682037.1:c.85G= ENSP00000508289.1:p.Val29=
ENST00000682219.1:n.964G=
ENST00000682226.1:n.419G=
ENST00000682487.1:n.419G=
ENST00000683330.1:n.419G=
ENST00000683703.1:n.419G=
ENST00000683837.1:n.419G=
ENST00000684737.1:n.419G=
ENST00000358385.12:c.85G= MANE Select ENSP00000351155.7:p.Val29=
ENST00000674288.1:c.85G= ENSP00000501522.1:p.Val29=
ENST00000674478.1:n.419G=
ENST00000674503.1:c.-165G= ENSP00000501520.1:n.-165G=
ENST00000358385.10:c.85G= ENSP00000351155.6:p.Val29=
ENST00000441560.6:c.85G= ENSP00000413675.2:p.Val29=
ENST00000553509.1:c.85G= ENSP00000450989.1:p.Val29=
ENST00000554886.1:c.-150-3060G= ENSP00000452074.1:n.-150-3060G=
ENST00000555960.5:c.85G= ENSP00000452506.1:p.Val29=
ENST00000556478.2:n.589G=
ENST00000557735.1:c.-165G= ENSP00000451015.1:n.-165G=
NM_001127713.1:c.85G= NP_001121185.1:p.Val29=
NM_015915.4:c.85G= NP_056999.2:p.Val29=
NM_181598.3:c.85G= NP_853629.2:p.Val29=
NM_015915.5:c.85G= MANE Select NP_056999.2:p.Val29=
NM_181598.4:c.85G= NP_853629.2:p.Val29=