Canonical Allele Identifier: CA480666139
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65632504T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238724T>C , CM000674.2:g.65238724T>C GRCh38
NC_000012.11:g.65632504T>C , CM000674.1:g.65632504T>C GRCh37
NC_000012.10:g.63918771T>C NCBI36
NG_016210.1:g.74154T>C
NG_016210.2:g.74154T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1831T>C MANE Select ENSP00000308369.2:p.Leu611=
ENST00000308330.2:c.1831T>C ENSP00000308369.2:p.Leu611=
NM_001167614.1:c.1828T>C NP_001161086.1:p.Leu610=
NM_014319.4:c.1831T>C NP_055134.2:p.Leu611=
NM_014319.5:c.1831T>C MANE Select NP_055134.2:p.Leu611=
NM_001167614.2:c.1828T>C NP_001161086.1:p.Leu610=