Canonical Allele Identifier: CA2619670885
Gene: LEMD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65246895_65246896insCAA , CM000674.2:g.65246895_65246896insCAA GRCh38
NC_000012.11:g.65640675_65640676insCAA , CM000674.1:g.65640675_65640676insCAA GRCh37
NC_000012.10:g.63926942_63926943insCAA NCBI36
NG_016210.1:g.82325_82326insCAA
NG_016210.2:g.82325_82326insCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.*570_*571insCAA MANE Select ENSP00000308369.2:n.*570_*571insCAA
ENST00000308330.2:c.*570_*571insCAA ENSP00000308369.2:n.*570_*571insCAA
NM_001167614.1:c.*570_*571insCAA NP_001161086.1:n.*570_*571insCAA
NM_014319.4:c.*570_*571insCAA NP_055134.2:n.*570_*571insCAA
NM_014319.5:c.*570_*571insCAA MANE Select NP_055134.2:n.*570_*571insCAA
NM_001167614.2:c.*570_*571insCAA NP_001161086.1:n.*570_*571insCAA