Canonical Allele Identifier: CA139831076

Gene: LGSN

Linked Data

• dbSNP Id: rs969408200
• gnomAD v3: 6-63304934-G-A
• gnomAD v4: 6-63304934-G-A
• MyVariant Identifiers: chr6:g.64014839G>A (hg19) ; chr6:g.63304934G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.63304934G>A , CM000668.2:g.63304934G>A	GRCh38
NC_000006.11:g.64014839G>A , CM000668.1:g.64014839G>A	GRCh37
NC_000006.10:g.64072798G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000370657.9:c.31-9889C>T MANE Select	ENSP00000359691.4:n.31-9889C>T
ENST00000370657.8:c.31-9889C>T	ENSP00000359691.4:n.31-9889C>T
ENST00000370658.9:c.31-9889C>T	ENSP00000359692.5:n.31-9889C>T
ENST00000485906.6:c.31-9889C>T	ENSP00000431246.2:n.31-9889C>T
ENST00000622415.1:c.31-9889C>T	ENSP00000479173.1:n.31-9889C>T
NM_001143940.1:c.31-9889C>T	NP_001137412.1:n.31-9889C>T
NM_016571.2:c.31-9889C>T	NP_057655.2:n.31-9889C>T
XM_011535889.1:c.85-9889C>T	XP_011534191.1:n.85-9889C>T
XM_011535890.1:c.-42-9889C>T	XP_011534192.1:n.-42-9889C>T
XM_011535891.1:c.-42-9889C>T	XP_011534193.1:n.-42-9889C>T
XM_011535892.1:c.-42-9889C>T	XP_011534194.1:n.-42-9889C>T
XM_011535889.3:c.85-9889C>T	XP_011534191.1:n.85-9889C>T
XM_011535892.3:c.-42-9889C>T	XP_011534194.1:n.-42-9889C>T
XM_017010929.2:c.85-9889C>T	XP_016866418.1:n.85-9889C>T
XM_017010930.2:c.85-9889C>T	XP_016866419.1:n.85-9889C>T
XM_017010931.2:c.-42-9889C>T	XP_016866420.1:n.-42-9889C>T
NM_016571.3:c.31-9889C>T MANE Select	NP_057655.2:n.31-9889C>T
NM_001143940.2:c.31-9889C>T	NP_001137412.1:n.31-9889C>T