Canonical Allele Identifier: CA2136274937

Gene: ATL1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50613227C= , CM000676.2:g.50613227C=	GRCh38
NC_000014.8:g.51079945C= , CM000676.1:g.51079945C=	GRCh37
NC_000014.7:g.50149695C=	NCBI36
NG_009028.1:g.85146C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000553509.2:c.631-32C=	ENSP00000450989.2:n.631-32C=
ENST00000556478.3:c.631-32C=	ENSP00000501428.2:n.631-32C=
ENST00000682037.1:c.631-32C=	ENSP00000508289.1:n.631-32C=
ENST00000682219.1:n.1969-32C=
ENST00000682487.1:n.965-32C=
ENST00000683037.1:n.552-32C=
ENST00000683330.1:n.965-32C=
ENST00000683837.1:n.965-32C=
ENST00000358385.12:c.631-32C= MANE Select	ENSP00000351155.7:n.631-32C=
ENST00000674288.1:c.*1923-32C=	ENSP00000501522.1:n.*1923-32C=
ENST00000358385.10:c.631-32C=	ENSP00000351155.6:n.631-32C=
ENST00000441560.6:c.631-32C=	ENSP00000413675.2:n.631-32C=
ENST00000554886.1:c.199-32C=	ENSP00000452074.1:n.199-32C=
NM_001127713.1:c.631-32C=	NP_001121185.1:n.631-32C=
NM_015915.4:c.631-32C=	NP_056999.2:n.631-32C=
NM_181598.3:c.631-32C=	NP_853629.2:n.631-32C=
NM_015915.5:c.631-32C= MANE Select	NP_056999.2:n.631-32C=
NM_181598.4:c.631-32C=	NP_853629.2:n.631-32C=