Canonical Allele Identifier: CA385671173
Gene: LEMD3 HGNC NCBI

Linked Data

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

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000308330.3:c.1829T>A MANE Select ENSP00000308369.2:p.Phe610Tyr
ENST00000308330.2:c.1829T>A ENSP00000308369.2:p.Phe610Tyr
NM_001167614.1:c.1826T>A NP_001161086.1:p.Phe609Tyr
NM_014319.4:c.1829T>A NP_055134.2:p.Phe610Tyr
NM_014319.5:c.1829T>A MANE Select NP_055134.2:p.Phe610Tyr
NM_001167614.2:c.1826T>A NP_001161086.1:p.Phe609Tyr
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