Canonical Allele Identifier: CA480666267

Gene: LEMD3

Linked Data

• MyVariant Identifiers: chr12:g.65633809A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65240029A>T , CM000674.2:g.65240029A>T	GRCh38
NC_000012.11:g.65633809A>T , CM000674.1:g.65633809A>T	GRCh37
NC_000012.10:g.63920076A>T	NCBI36
NG_016210.1:g.75459A>T
NG_016210.2:g.75459A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.2022A>T MANE Select	ENSP00000308369.2:p.Ile674=
ENST00000308330.2:c.2022A>T	ENSP00000308369.2:p.Ile674=
NM_001167614.1:c.2019A>T	NP_001161086.1:p.Ile673=
NM_014319.4:c.2022A>T	NP_055134.2:p.Ile674=
NM_014319.5:c.2022A>T MANE Select	NP_055134.2:p.Ile674=
NM_001167614.2:c.2019A>T	NP_001161086.1:p.Ile673=