Canonical Allele Identifier: CA2434042996

Gene: LAS1L

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.65523637G= , CM000685.2:g.65523637G=	GRCh38
NC_000023.10:g.64743517G= , CM000685.1:g.64743517G=	GRCh37
NC_000023.9:g.64660242G=	NCBI36
NG_016369.1:g.16170C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374811.8:c.1371C= MANE Select	ENSP00000363944.3:p.Ser457=
ENST00000676986.1:c.1320C=	ENSP00000503577.1:p.Ser440=
ENST00000677056.1:c.*774C=	ENSP00000504224.1:n.*774C=
ENST00000677087.1:c.1023C=	ENSP00000503907.1:p.Ser341=
ENST00000677154.1:n.1403C=
ENST00000677834.1:n.1359C=
ENST00000677969.1:c.1320C=	ENSP00000503410.1:p.Ser440=
ENST00000677986.1:n.2304C=
ENST00000678074.1:n.2351C=
ENST00000678173.1:n.1454C=
ENST00000678547.1:n.1645C=
ENST00000678570.1:c.1413C=	ENSP00000504558.1:p.Ser471=
ENST00000678705.1:n.2439C=
ENST00000678823.1:c.1371C=	ENSP00000503795.1:p.Ser457=
ENST00000678848.1:n.4627C=
ENST00000678956.1:c.1371C=	ENSP00000504653.1:p.Ser457=
ENST00000679056.1:n.1466C=
ENST00000679116.1:n.1587C=
ENST00000679261.1:n.1456C=
ENST00000679277.1:n.1924C=
ENST00000374804.9:c.1194C=	ENSP00000363937.5:p.Ser398=
ENST00000374807.9:c.1320C=	ENSP00000363940.5:p.Ser440=
ENST00000374811.7:c.1371C=	ENSP00000363944.3:p.Ser457=
ENST00000484069.1:c.*385C=	ENSP00000473471.1:n.*385C=
NM_001170649.1:c.1320C=	NP_001164120.1:p.Ser440=
NM_001170650.1:c.1194C=	NP_001164121.1:p.Ser398=
NM_031206.4:c.1371C=	NP_112483.1:p.Ser457=
XM_005262301.1:c.1371C=	XP_005262358.1:p.Ser457=
XM_005262304.1:c.1371C=	XP_005262361.1:p.Ser457=
XM_005262305.3:c.1371C=	XP_005262362.1:p.Ser457=
XM_005262306.3:c.1371C=	XP_005262363.1:p.Ser457=
XM_005262307.1:c.465C=	XP_005262364.1:p.Ser155=
XM_011531045.1:c.1245C=	XP_011529347.1:p.Ser415=
XM_011531046.1:c.1371C=	XP_011529348.1:p.Ser457=
XR_244504.1:n.1447C=
XR_430522.1:n.1447C=
XR_938411.1:n.1447C=
XR_938412.1:n.1447C=
XM_005262301.2:c.1371C=	XP_005262358.1:p.Ser457=
XM_005262304.2:c.1371C=	XP_005262361.1:p.Ser457=
XM_005262305.4:c.1371C=	XP_005262362.1:p.Ser457=
XM_005262306.4:c.1371C=	XP_005262363.1:p.Ser457=
XM_011531045.2:c.1245C=	XP_011529347.1:p.Ser415=
XM_011531046.2:c.1371C=	XP_011529348.1:p.Ser457=
XM_017029877.2:c.1320C=	XP_016885366.1:p.Ser440=
XM_017029878.2:c.1320C=	XP_016885367.1:p.Ser440=
XM_017029879.2:c.465C=	XP_016885368.1:p.Ser155=
XM_017029880.2:c.414C=	XP_016885369.1:p.Ser138=
XR_001755730.2:n.1383C=
XR_001755731.2:n.1434C=
XR_001755732.2:n.1434C=
XR_001755733.2:n.1383C=
XR_244504.2:n.1434C=
XR_430522.2:n.1434C=
XR_938412.2:n.1434C=
NM_001375328.1:c.1371C=	NP_001362257.1:p.Ser457=
NM_001375329.1:c.1371C=	NP_001362258.1:p.Ser457=
NM_001375330.1:c.1371C=	NP_001362259.1:p.Ser457=
NM_001375331.1:c.1320C=	NP_001362260.1:p.Ser440=
NM_001375332.1:c.414C=	NP_001362261.1:p.Ser138=
NM_001375333.1:c.1320C=	NP_001362262.1:p.Ser440=
NM_001375334.1:c.1371C=	NP_001362263.1:p.Ser457=
NM_001375335.1:c.1371C=	NP_001362264.1:p.Ser457=
NM_001375336.1:c.1320C=	NP_001362265.1:p.Ser440=
NM_001375337.1:c.1320C=	NP_001362266.1:p.Ser440=
NM_031206.7:c.1371C= MANE Select	NP_112483.1:p.Ser457=
NR_164681.1:n.1443C=
NM_001170649.2:c.1320C=	NP_001164120.1:p.Ser440=
NM_001170650.2:c.1194C=	NP_001164121.1:p.Ser398=