Canonical Allele Identifier: CA2579661270

Gene: LAS1L

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65524036dup , CM000685.2:g.65524036dup	GRCh38
NC_000023.10:g.64743916dup , CM000685.1:g.64743916dup	GRCh37
NC_000023.9:g.64660641dup	NCBI36
NG_016369.1:g.15771dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000374811.8:c.1300+20dup MANE Select	ENSP00000363944.3:n.1300+20dup
ENST00000676986.1:c.1249+20dup	ENSP00000503577.1:n.1249+20dup
ENST00000677056.1:c.*703+20dup	ENSP00000504224.1:n.*703+20dup
ENST00000677087.1:c.952+20dup	ENSP00000503907.1:n.952+20dup
ENST00000677154.1:n.1332+20dup
ENST00000677834.1:n.1288+20dup
ENST00000677969.1:c.1249+20dup	ENSP00000503410.1:n.1249+20dup
ENST00000677986.1:n.2233+20dup
ENST00000678074.1:n.1952dup
ENST00000678173.1:n.1383+20dup
ENST00000678547.1:n.1574+20dup
ENST00000678570.1:c.1342+20dup	ENSP00000504558.1:n.1342+20dup
ENST00000678705.1:n.2040dup
ENST00000678823.1:c.1300+20dup	ENSP00000503795.1:n.1300+20dup
ENST00000678848.1:n.4228dup
ENST00000678956.1:c.1300+20dup	ENSP00000504653.1:n.1300+20dup
ENST00000679056.1:n.1395+20dup
ENST00000679116.1:n.1516+20dup
ENST00000679261.1:n.1385+20dup
ENST00000679277.1:n.1684+20dup
ENST00000374804.9:c.1123+20dup	ENSP00000363937.5:n.1123+20dup
ENST00000374807.9:c.1249+20dup	ENSP00000363940.5:n.1249+20dup
ENST00000374811.7:c.1300+20dup	ENSP00000363944.3:n.1300+20dup
ENST00000484069.1:c.*314+20dup	ENSP00000473471.1:n.*314+20dup
NM_001170649.1:c.1249+20dup	NP_001164120.1:n.1249+20dup
NM_001170650.1:c.1123+20dup	NP_001164121.1:n.1123+20dup
NM_031206.4:c.1300+20dup	NP_112483.1:n.1300+20dup
XM_005262301.1:c.1300+20dup	XP_005262358.1:n.1300+20dup
XM_005262304.1:c.1300+20dup	XP_005262361.1:n.1300+20dup
XM_005262305.3:c.1300+20dup	XP_005262362.1:n.1300+20dup
XM_005262306.3:c.1300+20dup	XP_005262363.1:n.1300+20dup
XM_005262307.1:c.394+20dup	XP_005262364.1:n.394+20dup
XM_011531045.1:c.1174+20dup	XP_011529347.1:n.1174+20dup
XM_011531046.1:c.1300+20dup	XP_011529348.1:n.1300+20dup
XR_244504.1:n.1376+20dup
XR_430522.1:n.1376+20dup
XR_938411.1:n.1376+20dup
XR_938412.1:n.1376+20dup
XM_005262301.2:c.1300+20dup	XP_005262358.1:n.1300+20dup
XM_005262304.2:c.1300+20dup	XP_005262361.1:n.1300+20dup
XM_005262305.4:c.1300+20dup	XP_005262362.1:n.1300+20dup
XM_005262306.4:c.1300+20dup	XP_005262363.1:n.1300+20dup
XM_011531045.2:c.1174+20dup	XP_011529347.1:n.1174+20dup
XM_011531046.2:c.1300+20dup	XP_011529348.1:n.1300+20dup
XM_017029877.2:c.1249+20dup	XP_016885366.1:n.1249+20dup
XM_017029878.2:c.1249+20dup	XP_016885367.1:n.1249+20dup
XM_017029879.2:c.394+20dup	XP_016885368.1:n.394+20dup
XM_017029880.2:c.343+20dup	XP_016885369.1:n.343+20dup
XR_001755730.2:n.1312+20dup
XR_001755731.2:n.1363+20dup
XR_001755732.2:n.1363+20dup
XR_001755733.2:n.1312+20dup
XR_244504.2:n.1363+20dup
XR_430522.2:n.1363+20dup
XR_938412.2:n.1363+20dup
NM_001375328.1:c.1300+20dup	NP_001362257.1:n.1300+20dup
NM_001375329.1:c.1300+20dup	NP_001362258.1:n.1300+20dup
NM_001375330.1:c.1300+20dup	NP_001362259.1:n.1300+20dup
NM_001375331.1:c.1249+20dup	NP_001362260.1:n.1249+20dup
NM_001375332.1:c.343+20dup	NP_001362261.1:n.343+20dup
NM_001375333.1:c.1249+20dup	NP_001362262.1:n.1249+20dup
NM_001375334.1:c.1300+20dup	NP_001362263.1:n.1300+20dup
NM_001375335.1:c.1300+20dup	NP_001362264.1:n.1300+20dup
NM_001375336.1:c.1249+20dup	NP_001362265.1:n.1249+20dup
NM_001375337.1:c.1249+20dup	NP_001362266.1:n.1249+20dup
NM_031206.7:c.1300+20dup MANE Select	NP_112483.1:n.1300+20dup
NR_164681.1:n.1372+20dup
NM_001170649.2:c.1249+20dup	NP_001164120.1:n.1249+20dup
NM_001170650.2:c.1123+20dup	NP_001164121.1:n.1123+20dup