Canonical Allele Identifier: CA2615933693

Gene: LAYN

Linked Data

• gnomAD v4: 11-111540785-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.111540785C>T , CM000673.2:g.111540785C>T	GRCh38
NC_000011.9:g.111411510C>T , CM000673.1:g.111411510C>T	GRCh37
NC_000011.8:g.110916720C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000375614.7:c.-59C>T MANE Select	ENSP00000364764.2:n.-59C>T
ENST00000375614.6:c.-59C>T	ENSP00000364764.2:n.-59C>T
ENST00000375615.7:c.-59C>T	ENSP00000364765.3:n.-59C>T
ENST00000436913.6:c.-336C>T	ENSP00000392942.2:n.-336C>T
ENST00000525126.5:c.-59C>T	ENSP00000434328.1:n.-59C>T
ENST00000525866.5:c.-59C>T	ENSP00000434300.1:n.-59C>T
ENST00000533265.5:c.-59C>T	ENSP00000434972.1:n.-59C>T
ENST00000533999.5:c.-348+451C>T	ENSP00000432434.1:n.-348+451C>T
NM_001258390.1:c.-59C>T	NP_001245319.1:n.-59C>T
NM_001258391.1:c.-336C>T	NP_001245320.1:n.-336C>T
NM_178834.4:c.-59C>T	NP_849156.1:n.-59C>T
XM_011542625.1:c.-348+451C>T	XP_011540927.1:n.-348+451C>T
NM_001318799.1:c.-348+451C>T	NP_001305728.1:n.-348+451C>T
NM_001258390.2:c.-59C>T	NP_001245319.1:n.-59C>T
NM_001258391.2:c.-336C>T	NP_001245320.1:n.-336C>T
NM_178834.5:c.-59C>T MANE Select	NP_849156.1:n.-59C>T