Canonical Allele Identifier: CA385676655

Gene: LEMD3

Linked Data

• MyVariant Identifiers: chr12:g.65640019C>A (hg19) ; chr12:g.65246239C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65246239C>A , CM000674.2:g.65246239C>A	GRCh38
NC_000012.11:g.65640019C>A , CM000674.1:g.65640019C>A	GRCh37
NC_000012.10:g.63926286C>A	NCBI36
NG_016210.1:g.81669C>A
NG_016210.2:g.81669C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308330.3:c.2650C>A MANE Select	ENSP00000308369.2:p.Pro884Thr
ENST00000308330.2:c.2650C>A	ENSP00000308369.2:p.Pro884Thr
ENST00000539442.1:n.632C>A
ENST00000544506.1:n.370C>A
ENST00000545026.1:n.468C>A
NM_001167614.1:c.2647C>A	NP_001161086.1:p.Pro883Thr
NM_014319.4:c.2650C>A	NP_055134.2:p.Pro884Thr
NM_014319.5:c.2650C>A MANE Select	NP_055134.2:p.Pro884Thr
NM_001167614.2:c.2647C>A	NP_001161086.1:p.Pro883Thr