Canonical Allele Identifier: CA671668166

Gene: LAYN

Linked Data

• dbSNP Id: rs1280345548
• gnomAD v4: 11-111540790-G-A
• MyVariant Identifiers: chr11:g.111411515G>A (hg19) ; chr11:g.111540790G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.111540790G>A , CM000673.2:g.111540790G>A	GRCh38
NC_000011.9:g.111411515G>A , CM000673.1:g.111411515G>A	GRCh37
NC_000011.8:g.110916725G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375614.7:c.-54G>A MANE Select	ENSP00000364764.2:n.-54G>A
ENST00000375614.6:c.-54G>A	ENSP00000364764.2:n.-54G>A
ENST00000375615.7:c.-54G>A	ENSP00000364765.3:n.-54G>A
ENST00000436913.6:c.-331G>A	ENSP00000392942.2:n.-331G>A
ENST00000525126.5:c.-54G>A	ENSP00000434328.1:n.-54G>A
ENST00000525866.5:c.-54G>A	ENSP00000434300.1:n.-54G>A
ENST00000533265.5:c.-54G>A	ENSP00000434972.1:n.-54G>A
ENST00000533999.5:c.-348+456G>A	ENSP00000432434.1:n.-348+456G>A
NM_001258390.1:c.-54G>A	NP_001245319.1:n.-54G>A
NM_001258391.1:c.-331G>A	NP_001245320.1:n.-331G>A
NM_178834.4:c.-54G>A	NP_849156.1:n.-54G>A
XM_011542625.1:c.-348+456G>A	XP_011540927.1:n.-348+456G>A
NM_001318799.1:c.-348+456G>A	NP_001305728.1:n.-348+456G>A
NM_001258390.2:c.-54G>A	NP_001245319.1:n.-54G>A
NM_001258391.2:c.-331G>A	NP_001245320.1:n.-331G>A
NM_178834.5:c.-54G>A MANE Select	NP_849156.1:n.-54G>A