Canonical Allele Identifier: CA385673343

Gene: LEMD3

Linked Data

• gnomAD v4: 12-65170092-C-T
• MyVariant Identifiers: chr12:g.65563872C>T (hg19) ; chr12:g.65170092C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65170092C>T , CM000674.2:g.65170092C>T	GRCh38
NC_000012.11:g.65563872C>T , CM000674.1:g.65563872C>T	GRCh37
NC_000012.10:g.63850139C>T	NCBI36
NG_016210.1:g.5522C>T
NG_016210.2:g.5522C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.496C>T MANE Select	ENSP00000308369.2:p.Gln166Ter
ENST00000308330.2:c.496C>T	ENSP00000308369.2:p.Gln166Ter
ENST00000541171.1:n.510C>T
NM_001167614.1:c.496C>T	NP_001161086.1:p.Gln166Ter
NM_014319.4:c.496C>T	NP_055134.2:p.Gln166Ter
NM_014319.5:c.496C>T MANE Select	NP_055134.2:p.Gln166Ter
NM_001167614.2:c.496C>T	NP_001161086.1:p.Gln166Ter