Canonical Allele Identifier: CA2136287672

Gene: ATL1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50628345T= , CM000676.2:g.50628345T=	GRCh38
NC_000014.8:g.51095063T= , CM000676.1:g.51095063T=	GRCh37
NC_000014.7:g.50164813T=	NCBI36
NG_009028.1:g.100264T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553509.2:c.1434T=	ENSP00000450989.2:p.Asn478=
ENST00000556478.3:c.1434T=	ENSP00000501428.2:p.Asn478=
ENST00000682037.1:c.1434T=	ENSP00000508289.1:p.Asn478=
ENST00000682219.1:n.2772T=
ENST00000683037.1:n.1355T=
ENST00000683330.1:n.1768T=
ENST00000358385.12:c.1434T= MANE Select	ENSP00000351155.7:p.Asn478=
ENST00000674288.1:c.*2726T=	ENSP00000501522.1:n.*2726T=
ENST00000358385.10:c.1434T=	ENSP00000351155.6:p.Asn478=
ENST00000441560.6:c.1434T=	ENSP00000413675.2:p.Asn478=
ENST00000556067.1:c.180T=	ENSP00000451100.1:p.Asn60=
NM_001127713.1:c.1434T=	NP_001121185.1:p.Asn478=
NM_015915.4:c.1434T=	NP_056999.2:p.Asn478=
NM_181598.3:c.1434T=	NP_853629.2:p.Asn478=
NM_015915.5:c.1434T= MANE Select	NP_056999.2:p.Asn478=
NM_181598.4:c.1434T=	NP_853629.2:p.Asn478=