Canonical Allele Identifier: CA2624804626

Gene: ATL1

Linked Data

• gnomAD v4: 14-50587880-A-AAG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.50587880_50587881insAG , CM000676.2:g.50587880_50587881insAG	GRCh38
NC_000014.8:g.51054598_51054599insAG , CM000676.1:g.51054598_51054599insAG	GRCh37
NC_000014.7:g.50124348_50124349insAG	NCBI36
NG_009028.1:g.59799_59800insAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000553509.2:c.84_85insAG	ENSP00000450989.2:p.Val29ArgfsTer2
ENST00000553746.2:n.285_286insAG
ENST00000556478.3:c.84_85insAG	ENSP00000501428.2:p.Val29ArgfsTer2
ENST00000682037.1:c.84_85insAG	ENSP00000508289.1:p.Val29ArgfsTer2
ENST00000682219.1:n.963_964insAG
ENST00000682226.1:n.418_419insAG
ENST00000682487.1:n.418_419insAG
ENST00000683330.1:n.418_419insAG
ENST00000683703.1:n.418_419insAG
ENST00000683837.1:n.418_419insAG
ENST00000684737.1:n.418_419insAG
ENST00000358385.12:c.84_85insAG MANE Select	ENSP00000351155.7:p.Val29ArgfsTer2
ENST00000674288.1:c.84_85insAG	ENSP00000501522.1:p.Val29ArgfsTer2
ENST00000674478.1:n.418_419insAG
ENST00000674503.1:c.-166_-165insAG	ENSP00000501520.1:n.-166_-165insAG
ENST00000358385.10:c.84_85insAG	ENSP00000351155.6:p.Val29ArgfsTer2
ENST00000441560.6:c.84_85insAG	ENSP00000413675.2:p.Val29ArgfsTer2
ENST00000553509.1:c.84_85insAG	ENSP00000450989.1:p.Val29ArgfsTer2
ENST00000554886.1:c.-150-3061_-150-3060insAG	ENSP00000452074.1:n.-150-3061_-150-3060in...
ENST00000555960.5:c.84_85insAG	ENSP00000452506.1:p.Val29ArgfsTer2
ENST00000556478.2:n.588_589insAG
ENST00000557735.1:c.-166_-165insAG	ENSP00000451015.1:n.-166_-165insAG
NM_001127713.1:c.84_85insAG	NP_001121185.1:p.Val29ArgfsTer2
NM_015915.4:c.84_85insAG	NP_056999.2:p.Val29ArgfsTer2
NM_181598.3:c.84_85insAG	NP_853629.2:p.Val29ArgfsTer2
NM_015915.5:c.84_85insAG MANE Select	NP_056999.2:p.Val29ArgfsTer2
NM_181598.4:c.84_85insAG	NP_853629.2:p.Val29ArgfsTer2