Canonical Allele Identifier: CA2830541102

Gene: LGSN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63280676_63280677insG , CM000668.2:g.63280676_63280677insG	GRCh38
NC_000006.11:g.63990581_63990582insG , CM000668.1:g.63990581_63990582insG	GRCh37
NC_000006.10:g.64048540_64048541insG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370657.9:c.874_875insC MANE Select	ENSP00000359691.4:p.Val292AlafsTer6
ENST00000370657.8:c.874_875insC	ENSP00000359691.4:p.Val292AlafsTer6
ENST00000370658.9:c.530-77_530-76insC	ENSP00000359692.5:n.530-77_530-76insC
ENST00000485906.6:c.529+345_529+346insC	ENSP00000431246.2:n.529+345_529+346insC
ENST00000622415.1:c.956_957insC	ENSP00000479173.1:n.956_957insC
NM_001143940.1:c.530-77_530-76insC	NP_001137412.1:n.530-77_530-76insC
NM_016571.2:c.874_875insC	NP_057655.2:p.Val292AlafsTer6
XM_011535889.1:c.1117_1118insC	XP_011534191.1:p.Val373AlafsTer6
XM_011535890.1:c.991_992insC	XP_011534192.1:p.Val331AlafsTer6
XM_011535891.1:c.991_992insC	XP_011534193.1:p.Val331AlafsTer6
XM_011535892.1:c.991_992insC	XP_011534194.1:p.Val331AlafsTer6
XM_011535893.1:c.658_659insC	XP_011534195.1:p.Val220AlafsTer6
XM_011535889.3:c.1117_1118insC	XP_011534191.1:p.Val373AlafsTer6
XM_011535892.3:c.991_992insC	XP_011534194.1:p.Val331AlafsTer6
XM_017010929.2:c.1117_1118insC	XP_016866418.1:p.Val373AlafsTer6
XM_017010930.2:c.1117_1118insC	XP_016866419.1:p.Val373AlafsTer6
XM_017010931.2:c.802_803insC	XP_016866420.1:p.Val268AlafsTer6
NM_016571.3:c.874_875insC MANE Select	NP_057655.2:p.Val292AlafsTer6
NM_001143940.2:c.530-77_530-76insC	NP_001137412.1:n.530-77_530-76insC