Canonical Allele Identifier: CA385671918
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65239977C>G , CM000674.2:g.65239977C>G GRCh38
NC_000012.11:g.65633757C>G , CM000674.1:g.65633757C>G GRCh37
NC_000012.10:g.63920024C>G NCBI36
NG_016210.1:g.75407C>G
NG_016210.2:g.75407C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000308330.3:c.1970C>G MANE Select ENSP00000308369.2:p.Thr657Arg
ENST00000308330.2:c.1970C>G ENSP00000308369.2:p.Thr657Arg
NM_001167614.1:c.1967C>G NP_001161086.1:p.Thr656Arg
NM_014319.4:c.1970C>G NP_055134.2:p.Thr657Arg
NM_014319.5:c.1970C>G MANE Select NP_055134.2:p.Thr657Arg
NM_001167614.2:c.1967C>G NP_001161086.1:p.Thr656Arg