Canonical Allele Identifier: CA2042444290
Gene: LEMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238559A= , CM000674.2:g.65238559A= GRCh38
NC_000012.11:g.65632339A= , CM000674.1:g.65632339A= GRCh37
NC_000012.10:g.63918606A= NCBI36
NG_016210.1:g.73989A=
NG_016210.2:g.73989A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1753A= MANE Select ENSP00000308369.2:p.Asn585=
ENST00000308330.2:c.1753A= ENSP00000308369.2:p.Asn585=
NM_001167614.1:c.1750A= NP_001161086.1:p.Asn584=
NM_014319.4:c.1753A= NP_055134.2:p.Asn585=
NM_014319.5:c.1753A= MANE Select NP_055134.2:p.Asn585=
NM_001167614.2:c.1750A= NP_001161086.1:p.Asn584=