Canonical Allele Identifier: CA2136287770

Gene: ATL1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50628419_50628420delinsTG , CM000676.2:g.50628419_50628420delinsTG	GRCh38
NC_000014.8:g.51095137_51095138delinsTG , CM000676.1:g.51095137_51095138delinsTG	GRCh37
NC_000014.7:g.50164887_50164888delinsTG	NCBI36
NG_009028.1:g.100338_100339delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000553509.2:c.1508_1509delinsTG	ENSP00000450989.2:p.Leu503=
ENST00000556478.3:c.1508_1509delinsTG	ENSP00000501428.2:p.Leu503=
ENST00000682037.1:c.1508_1509delinsTG	ENSP00000508289.1:p.Leu503=
ENST00000682219.1:n.2846_2847delinsTG
ENST00000683037.1:n.1429_1430delinsTG
ENST00000683330.1:n.1842_1843delinsTG
ENST00000358385.12:c.1508_1509delinsTG MANE Select	ENSP00000351155.7:p.Leu503=
ENST00000674288.1:c.*2800_*2801delinsTG	ENSP00000501522.1:n.*2800_*2801delinsTG
ENST00000358385.10:c.1508_1509delinsTG	ENSP00000351155.6:p.Leu503=
ENST00000441560.6:c.1508_1509delinsTG	ENSP00000413675.2:p.Leu503=
ENST00000556067.1:c.254_255delinsTG	ENSP00000451100.1:p.Leu85=
NM_001127713.1:c.1508_1509delinsTG	NP_001121185.1:p.Leu503=
NM_015915.4:c.1508_1509delinsTG	NP_056999.2:p.Leu503=
NM_181598.3:c.1508_1509delinsTG	NP_853629.2:p.Leu503=
NM_015915.5:c.1508_1509delinsTG MANE Select	NP_056999.2:p.Leu503=
NM_181598.4:c.1508_1509delinsTG	NP_853629.2:p.Leu503=