Canonical Allele Identifier: CA480666240
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65633752A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65239972A>C , CM000674.2:g.65239972A>C GRCh38
NC_000012.11:g.65633752A>C , CM000674.1:g.65633752A>C GRCh37
NC_000012.10:g.63920019A>C NCBI36
NG_016210.1:g.75402A>C
NG_016210.2:g.75402A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000308330.3:c.1965A>C MANE Select ENSP00000308369.2:p.Arg655=
ENST00000308330.2:c.1965A>C ENSP00000308369.2:p.Arg655=
NM_001167614.1:c.1962A>C NP_001161086.1:p.Arg654=
NM_014319.4:c.1965A>C NP_055134.2:p.Arg655=
NM_014319.5:c.1965A>C MANE Select NP_055134.2:p.Arg655=
NM_001167614.2:c.1962A>C NP_001161086.1:p.Arg654=