Canonical Allele Identifier: CA480666247
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65633761A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65239981A>G , CM000674.2:g.65239981A>G GRCh38
NC_000012.11:g.65633761A>G , CM000674.1:g.65633761A>G GRCh37
NC_000012.10:g.63920028A>G NCBI36
NG_016210.1:g.75411A>G
NG_016210.2:g.75411A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000308330.3:c.1974A>G MANE Select ENSP00000308369.2:p.Lys658=
ENST00000308330.2:c.1974A>G ENSP00000308369.2:p.Lys658=
NM_001167614.1:c.1971A>G NP_001161086.1:p.Lys657=
NM_014319.4:c.1974A>G NP_055134.2:p.Lys658=
NM_014319.5:c.1974A>G MANE Select NP_055134.2:p.Lys658=
NM_001167614.2:c.1971A>G NP_001161086.1:p.Lys657=