Canonical Allele Identifier: CA260791175

Gene: ATL1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50623384_50623385insAT , CM000676.2:g.50623384_50623385insAT	GRCh38
NC_000014.8:g.51090102_51090103insAT , CM000676.1:g.51090102_51090103insAT	GRCh37
NC_000014.7:g.50159852_50159853insAT	NCBI36
NG_009028.1:g.95303_95304insAT

Transcript Alleles

HGVS	Amino-acid Change
NM_015915.5:c.1119+136_1119+137insAT MANE Select	NP_056999.2:n.1119+136_1119+137insAT
ENST00000358385.12:c.1119+136_1119+137insAT MANE Select	ENSP00000351155.7:n.1119+136_1119+137insAT
NM_001127713.1:c.1119+136_1119+137insAT	NP_001121185.1:n.1119+136_1119+137insAT
NM_015915.4:c.1119+136_1119+137insAT	NP_056999.2:n.1119+136_1119+137insAT
NM_181598.3:c.1119+136_1119+137insAT	NP_853629.2:n.1119+136_1119+137insAT
NM_181598.4:c.1119+136_1119+137insAT	NP_853629.2:n.1119+136_1119+137insAT
ENST00000358385.10:c.1119+136_1119+137insAT	ENSP00000351155.6:n.1119+136_1119+137insAT
ENST00000441560.6:c.1119+136_1119+137insAT	ENSP00000413675.2:n.1119+136_1119+137insAT
ENST00000553509.2:c.1119+136_1119+137insAT	ENSP00000450989.2:n.1119+136_1119+137insAT
ENST00000555266.1:c.262+136_262+137insAT	ENSP00000450897.1:n.262+136_262+137insAT
ENST00000556478.3:c.1119+136_1119+137insAT	ENSP00000501428.2:n.1119+136_1119+137insAT
ENST00000674288.1:c.*2411+136_*2411+137insAT	ENSP00000501522.1:n.*2411+136_*2411+137insAT
ENST00000682037.1:c.1119+136_1119+137insAT	ENSP00000508289.1:n.1119+136_1119+137insAT
ENST00000682219.1:n.2457+136_2457+137insAT
ENST00000682487.1:n.2866_2867insAT
ENST00000683037.1:n.1040+136_1040+137insAT
ENST00000683330.1:n.1453+136_1453+137insAT
ENST00000683837.1:n.1589_1590insAT