Canonical Allele Identifier: CA385671175
Gene: LEMD3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.65632502T>G (hg19) chr12:g.65238722T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65238722T>G , CM000674.2:g.65238722T>G GRCh38
NC_000012.11:g.65632502T>G , CM000674.1:g.65632502T>G GRCh37
NC_000012.10:g.63918769T>G NCBI36
NG_016210.1:g.74152T>G
NG_016210.2:g.74152T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1829T>G MANE Select ENSP00000308369.2:p.Phe610Cys
ENST00000308330.2:c.1829T>G ENSP00000308369.2:p.Phe610Cys
NM_001167614.1:c.1826T>G NP_001161086.1:p.Phe609Cys
NM_014319.4:c.1829T>G NP_055134.2:p.Phe610Cys
NM_014319.5:c.1829T>G MANE Select NP_055134.2:p.Phe610Cys
NM_001167614.2:c.1826T>G NP_001161086.1:p.Phe609Cys
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