Canonical Allele Identifier: CA2619669557
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65239904A>T , CM000674.2:g.65239904A>T GRCh38
NC_000012.11:g.65633684A>T , CM000674.1:g.65633684A>T GRCh37
NC_000012.10:g.63919951A>T NCBI36
NG_016210.1:g.75334A>T
NG_016210.2:g.75334A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000308330.3:c.1922-25A>T MANE Select ENSP00000308369.2:n.1922-25A>T
ENST00000308330.2:c.1922-25A>T ENSP00000308369.2:n.1922-25A>T
NM_001167614.1:c.1919-25A>T NP_001161086.1:n.1919-25A>T
NM_014319.4:c.1922-25A>T NP_055134.2:n.1922-25A>T
NM_014319.5:c.1922-25A>T MANE Select NP_055134.2:n.1922-25A>T
NM_001167614.2:c.1919-25A>T NP_001161086.1:n.1919-25A>T