Canonical Allele Identifier: CA567169736

Gene: LGSN

Linked Data

• dbSNP Id: rs1194766610
• gnomAD v2: 6-64014862-C-T
• gnomAD v3: 6-63304957-C-T
• gnomAD v4: 6-63304957-C-T
• MyVariant Identifiers: chr6:g.64014862C>T (hg19) ; chr6:g.63304957C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63304957C>T , CM000668.2:g.63304957C>T	GRCh38
NC_000006.11:g.64014862C>T , CM000668.1:g.64014862C>T	GRCh37
NC_000006.10:g.64072821C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000370657.9:c.31-9912G>A MANE Select	ENSP00000359691.4:n.31-9912G>A
ENST00000370657.8:c.31-9912G>A	ENSP00000359691.4:n.31-9912G>A
ENST00000370658.9:c.31-9912G>A	ENSP00000359692.5:n.31-9912G>A
ENST00000485906.6:c.31-9912G>A	ENSP00000431246.2:n.31-9912G>A
ENST00000622415.1:c.31-9912G>A	ENSP00000479173.1:n.31-9912G>A
NM_001143940.1:c.31-9912G>A	NP_001137412.1:n.31-9912G>A
NM_016571.2:c.31-9912G>A	NP_057655.2:n.31-9912G>A
XM_011535889.1:c.85-9912G>A	XP_011534191.1:n.85-9912G>A
XM_011535890.1:c.-42-9912G>A	XP_011534192.1:n.-42-9912G>A
XM_011535891.1:c.-42-9912G>A	XP_011534193.1:n.-42-9912G>A
XM_011535892.1:c.-42-9912G>A	XP_011534194.1:n.-42-9912G>A
XM_011535889.3:c.85-9912G>A	XP_011534191.1:n.85-9912G>A
XM_011535892.3:c.-42-9912G>A	XP_011534194.1:n.-42-9912G>A
XM_017010929.2:c.85-9912G>A	XP_016866418.1:n.85-9912G>A
XM_017010930.2:c.85-9912G>A	XP_016866419.1:n.85-9912G>A
XM_017010931.2:c.-42-9912G>A	XP_016866420.1:n.-42-9912G>A
NM_016571.3:c.31-9912G>A MANE Select	NP_057655.2:n.31-9912G>A
NM_001143940.2:c.31-9912G>A	NP_001137412.1:n.31-9912G>A