Canonical Allele Identifier: CA385672037
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65633787A>C (hg19) chr12:g.65240007A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65240007A>C , CM000674.2:g.65240007A>C GRCh38
NC_000012.11:g.65633787A>C , CM000674.1:g.65633787A>C GRCh37
NC_000012.10:g.63920054A>C NCBI36
NG_016210.1:g.75437A>C
NG_016210.2:g.75437A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.2000A>C MANE Select ENSP00000308369.2:p.Tyr667Ser
ENST00000308330.2:c.2000A>C ENSP00000308369.2:p.Tyr667Ser
NM_001167614.1:c.1997A>C NP_001161086.1:p.Tyr666Ser
NM_014319.4:c.2000A>C NP_055134.2:p.Tyr667Ser
NM_014319.5:c.2000A>C MANE Select NP_055134.2:p.Tyr667Ser
NM_001167614.2:c.1997A>C NP_001161086.1:p.Tyr666Ser
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