Canonical Allele Identifier: CA389665128

Gene: ATL1

Linked Data

• ClinVar Variation Id: 2698667
• ClinVar RCV Id: RCV003502917
• MyVariant Identifiers: chr14:g.51054548G>A (hg19) ; chr14:g.50587830G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50587830G>A , CM000676.2:g.50587830G>A	GRCh38
NC_000014.8:g.51054548G>A , CM000676.1:g.51054548G>A	GRCh37
NC_000014.7:g.50124298G>A	NCBI36
NG_009028.1:g.59749G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553509.2:c.35-1G>A	ENSP00000450989.2:n.35-1G>A
ENST00000553746.2:n.236-1G>A
ENST00000556478.3:c.35-1G>A	ENSP00000501428.2:n.35-1G>A
ENST00000682037.1:c.35-1G>A	ENSP00000508289.1:n.35-1G>A
ENST00000682219.1:n.914-1G>A
ENST00000682226.1:n.369-1G>A
ENST00000682487.1:n.369-1G>A
ENST00000683330.1:n.369-1G>A
ENST00000683703.1:n.369-1G>A
ENST00000683837.1:n.369-1G>A
ENST00000684737.1:n.369-1G>A
ENST00000358385.12:c.35-1G>A MANE Select	ENSP00000351155.7:n.35-1G>A
ENST00000674288.1:c.35-1G>A	ENSP00000501522.1:n.35-1G>A
ENST00000674478.1:n.369-1G>A
ENST00000674503.1:c.-215-1G>A	ENSP00000501520.1:n.-215-1G>A
ENST00000358385.10:c.35-1G>A	ENSP00000351155.6:n.35-1G>A
ENST00000441560.6:c.35-1G>A	ENSP00000413675.2:n.35-1G>A
ENST00000553509.1:c.35-1G>A	ENSP00000450989.1:n.35-1G>A
ENST00000554886.1:c.-150-3111G>A	ENSP00000452074.1:n.-150-3111G>A
ENST00000555960.5:c.35-1G>A	ENSP00000452506.1:n.35-1G>A
ENST00000556478.2:n.539-1G>A
ENST00000557735.1:c.-215-1G>A	ENSP00000451015.1:n.-215-1G>A
NM_001127713.1:c.35-1G>A	NP_001121185.1:n.35-1G>A
NM_015915.4:c.35-1G>A	NP_056999.2:n.35-1G>A
NM_181598.3:c.35-1G>A	NP_853629.2:n.35-1G>A
NM_015915.5:c.35-1G>A MANE Select	NP_056999.2:n.35-1G>A
NM_181598.4:c.35-1G>A	NP_853629.2:n.35-1G>A