Canonical Allele Identifier: CA385671903
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65239974G>C , CM000674.2:g.65239974G>C GRCh38
NC_000012.11:g.65633754G>C , CM000674.1:g.65633754G>C GRCh37
NC_000012.10:g.63920021G>C NCBI36
NG_016210.1:g.75404G>C
NG_016210.2:g.75404G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000308330.3:c.1967G>C MANE Select ENSP00000308369.2:p.Trp656Ser
ENST00000308330.2:c.1967G>C ENSP00000308369.2:p.Trp656Ser
NM_001167614.1:c.1964G>C NP_001161086.1:p.Trp655Ser
NM_014319.4:c.1967G>C NP_055134.2:p.Trp656Ser
NM_014319.5:c.1967G>C MANE Select NP_055134.2:p.Trp656Ser
NM_001167614.2:c.1964G>C NP_001161086.1:p.Trp655Ser