Canonical Allele Identifier: CA1633185456

Gene: LGSN

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63304907A= , CM000668.2:g.63304907A=	GRCh38
NC_000006.11:g.64014812A= , CM000668.1:g.64014812A=	GRCh37
NC_000006.10:g.64072771A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000370657.9:c.31-9862T= MANE Select	ENSP00000359691.4:n.31-9862T=
ENST00000370657.8:c.31-9862T=	ENSP00000359691.4:n.31-9862T=
ENST00000370658.9:c.31-9862T=	ENSP00000359692.5:n.31-9862T=
ENST00000485906.6:c.31-9862T=	ENSP00000431246.2:n.31-9862T=
ENST00000622415.1:c.31-9862T=	ENSP00000479173.1:n.31-9862T=
NM_001143940.1:c.31-9862T=	NP_001137412.1:n.31-9862T=
NM_016571.2:c.31-9862T=	NP_057655.2:n.31-9862T=
XM_011535889.1:c.85-9862T=	XP_011534191.1:n.85-9862T=
XM_011535890.1:c.-42-9862T=	XP_011534192.1:n.-42-9862T=
XM_011535891.1:c.-42-9862T=	XP_011534193.1:n.-42-9862T=
XM_011535892.1:c.-42-9862T=	XP_011534194.1:n.-42-9862T=
XM_011535889.3:c.85-9862T=	XP_011534191.1:n.85-9862T=
XM_011535892.3:c.-42-9862T=	XP_011534194.1:n.-42-9862T=
XM_017010929.2:c.85-9862T=	XP_016866418.1:n.85-9862T=
XM_017010930.2:c.85-9862T=	XP_016866419.1:n.85-9862T=
XM_017010931.2:c.-42-9862T=	XP_016866420.1:n.-42-9862T=
NM_016571.3:c.31-9862T= MANE Select	NP_057655.2:n.31-9862T=
NM_001143940.2:c.31-9862T=	NP_001137412.1:n.31-9862T=