Canonical Allele Identifier: CA2042449601
Gene: LEMD3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65188445T= , CM000674.2:g.65188445T= GRCh38
NC_000012.11:g.65582225T= , CM000674.1:g.65582225T= GRCh37
NC_000012.10:g.63868492T= NCBI36
NG_016210.1:g.23875T=
NG_016210.2:g.23875T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1522+17327T= MANE Select ENSP00000308369.2:n.1522+17327T=
ENST00000308330.2:c.1522+17327T= ENSP00000308369.2:n.1522+17327T=
ENST00000541171.1:n.836+18027T=
NM_001167614.1:c.1522+17327T= NP_001161086.1:n.1522+17327T=
NM_014319.4:c.1522+17327T= NP_055134.2:n.1522+17327T=
NM_014319.5:c.1522+17327T= MANE Select NP_055134.2:n.1522+17327T=
NM_001167614.2:c.1522+17327T= NP_001161086.1:n.1522+17327T=