Canonical Allele Identifier: CA385671146
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65632489A>T (hg19) chr12:g.65238709A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238709A>T , CM000674.2:g.65238709A>T GRCh38
NC_000012.11:g.65632489A>T , CM000674.1:g.65632489A>T GRCh37
NC_000012.10:g.63918756A>T NCBI36
NG_016210.1:g.74139A>T
NG_016210.2:g.74139A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1816A>T MANE Select ENSP00000308369.2:p.Thr606Ser
ENST00000308330.2:c.1816A>T ENSP00000308369.2:p.Thr606Ser
NM_001167614.1:c.1813A>T NP_001161086.1:p.Thr605Ser
NM_014319.4:c.1816A>T NP_055134.2:p.Thr606Ser
NM_014319.5:c.1816A>T MANE Select NP_055134.2:p.Thr606Ser
NM_001167614.2:c.1813A>T NP_001161086.1:p.Thr605Ser
Search 100 bp 5'
Search 100 bp 3'