Canonical Allele Identifier: CA2624806219

Gene: ATL1

Linked Data

• gnomAD v4: 14-50628416-AGCTGGGAGCTGTAATAGACCAGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50628417_50628439del , CM000676.2:g.50628417_50628439del	GRCh38
NC_000014.8:g.51095135_51095157del , CM000676.1:g.51095135_51095157del	GRCh37
NC_000014.7:g.50164885_50164907del	NCBI36
NG_009028.1:g.100336_100358del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553509.2:c.1506_1528del	ENSP00000450989.2:p.Glu502AspfsTer?
ENST00000556478.3:c.1506_1528del	ENSP00000501428.2:p.Glu502AspfsTer?
ENST00000682037.1:c.1506_1528del	ENSP00000508289.1:p.Glu502AspfsTer?
ENST00000682219.1:n.2844_2866del
ENST00000683037.1:n.1427_1449del
ENST00000683330.1:n.1840_1862del
ENST00000358385.12:c.1506_1528del MANE Select	ENSP00000351155.7:p.Glu502AspfsTer13
ENST00000674288.1:c.*2798_*2820del	ENSP00000501522.1:n.*2798_*2820del
ENST00000358385.10:c.1506_1528del	ENSP00000351155.6:p.Glu502AspfsTer13
ENST00000441560.6:c.1506_1528del	ENSP00000413675.2:p.Glu502AspfsTer?
ENST00000556067.1:c.252_274del	ENSP00000451100.1:p.Glu84AspfsTer13
NM_001127713.1:c.1506_1528del	NP_001121185.1:p.Glu502AspfsTer?
NM_015915.4:c.1506_1528del	NP_056999.2:p.Glu502AspfsTer13
NM_181598.3:c.1506_1528del	NP_853629.2:p.Glu502AspfsTer?
NM_015915.5:c.1506_1528del MANE Select	NP_056999.2:p.Glu502AspfsTer13
NM_181598.4:c.1506_1528del	NP_853629.2:p.Glu502AspfsTer?