Canonical Allele Identifier: CA2434042990
Gene: LAS1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.65523616C= , CM000685.2:g.65523616C= GRCh38
NC_000023.10:g.64743496C= , CM000685.1:g.64743496C= GRCh37
NC_000023.9:g.64660221C= NCBI36
NG_016369.1:g.16191G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000374811.8:c.1392G= MANE Select ENSP00000363944.3:p.Arg464=
ENST00000676986.1:c.1341G= ENSP00000503577.1:p.Arg447=
ENST00000677056.1:c.*795G= ENSP00000504224.1:n.*795G=
ENST00000677087.1:c.1044G= ENSP00000503907.1:p.Arg348=
ENST00000677154.1:n.1424G=
ENST00000677834.1:n.1380G=
ENST00000677969.1:c.1341G= ENSP00000503410.1:p.Arg447=
ENST00000677986.1:n.2325G=
ENST00000678074.1:n.2372G=
ENST00000678173.1:n.1475G=
ENST00000678547.1:n.1666G=
ENST00000678570.1:c.1434G= ENSP00000504558.1:p.Arg478=
ENST00000678705.1:n.2460G=
ENST00000678823.1:c.1392G= ENSP00000503795.1:p.Arg464=
ENST00000678848.1:n.4648G=
ENST00000678956.1:c.1392G= ENSP00000504653.1:p.Arg464=
ENST00000679056.1:n.1487G=
ENST00000679116.1:n.1608G=
ENST00000679261.1:n.1477G=
ENST00000679277.1:n.1945G=
ENST00000374804.9:c.1215G= ENSP00000363937.5:p.Arg405=
ENST00000374807.9:c.1341G= ENSP00000363940.5:p.Arg447=
ENST00000374811.7:c.1392G= ENSP00000363944.3:p.Arg464=
ENST00000469091.1:c.2G=
ENST00000484069.1:c.*406G= ENSP00000473471.1:n.*406G=
NM_001170649.1:c.1341G= NP_001164120.1:p.Arg447=
NM_001170650.1:c.1215G= NP_001164121.1:p.Arg405=
NM_031206.4:c.1392G= NP_112483.1:p.Arg464=
XM_005262301.1:c.1392G= XP_005262358.1:p.Arg464=
XM_005262304.1:c.1392G= XP_005262361.1:p.Arg464=
XM_005262305.3:c.1392G= XP_005262362.1:p.Arg464=
XM_005262306.3:c.1392G= XP_005262363.1:p.Arg464=
XM_005262307.1:c.486G= XP_005262364.1:p.Arg162=
XM_011531045.1:c.1266G= XP_011529347.1:p.Arg422=
XM_011531046.1:c.1392G= XP_011529348.1:p.Arg464=
XR_244504.1:n.1468G=
XR_430522.1:n.1468G=
XR_938411.1:n.1468G=
XR_938412.1:n.1468G=
XM_005262301.2:c.1392G= XP_005262358.1:p.Arg464=
XM_005262304.2:c.1392G= XP_005262361.1:p.Arg464=
XM_005262305.4:c.1392G= XP_005262362.1:p.Arg464=
XM_005262306.4:c.1392G= XP_005262363.1:p.Arg464=
XM_011531045.2:c.1266G= XP_011529347.1:p.Arg422=
XM_011531046.2:c.1392G= XP_011529348.1:p.Arg464=
XM_017029877.2:c.1341G= XP_016885366.1:p.Arg447=
XM_017029878.2:c.1341G= XP_016885367.1:p.Arg447=
XM_017029879.2:c.486G= XP_016885368.1:p.Arg162=
XM_017029880.2:c.435G= XP_016885369.1:p.Arg145=
XR_001755730.2:n.1404G=
XR_001755731.2:n.1455G=
XR_001755732.2:n.1455G=
XR_001755733.2:n.1404G=
XR_244504.2:n.1455G=
XR_430522.2:n.1455G=
XR_938412.2:n.1455G=
NM_001375328.1:c.1392G= NP_001362257.1:p.Arg464=
NM_001375329.1:c.1392G= NP_001362258.1:p.Arg464=
NM_001375330.1:c.1392G= NP_001362259.1:p.Arg464=
NM_001375331.1:c.1341G= NP_001362260.1:p.Arg447=
NM_001375332.1:c.435G= NP_001362261.1:p.Arg145=
NM_001375333.1:c.1341G= NP_001362262.1:p.Arg447=
NM_001375334.1:c.1392G= NP_001362263.1:p.Arg464=
NM_001375335.1:c.1392G= NP_001362264.1:p.Arg464=
NM_001375336.1:c.1341G= NP_001362265.1:p.Arg447=
NM_001375337.1:c.1341G= NP_001362266.1:p.Arg447=
NM_031206.7:c.1392G= MANE Select NP_112483.1:p.Arg464=
NR_164681.1:n.1464G=
NM_001170649.2:c.1341G= NP_001164120.1:p.Arg447=
NM_001170650.2:c.1215G= NP_001164121.1:p.Arg405=